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Archives - Food and Drug Administration (FDA)

2017

12-22-2017
The Food and Drug Administration's Food-Recall Process Did Not Always Ensure the Safety of the Nation's Food Supply (A-01-16-01502)
09-28-2017
The Food and Drug Administration Generally Spent Prescription Drug User Fee Collections Appropriately (A-05-16-00040)

2016

Early Alert: The Food and Drug Administration Does Not Have an Efficient and Effective Food Recall Initiation Process (A-01-15-01500)

2014

10-21-2014
Penetration Test of the Food and Drug Administration's Computer Network (A-18-13-30331)

2011

06-21-2011
Review of the Food and Drug Administration's Monitoring of Imported Food Recalls (A-01-09-01500)

2009

08-12-2009
Review of the Food and Drug Administration's Monitoring of Pet Food Recalls (A-01-07-01503)

2007

06-07-2007
Emergency Response to Hurricanes Katrina and Rita: Audit of Food and Drug Administration's Award Process for a Contract With Marriott International, Inc. (A-03-06-00541)
05-22-2007
Emergency Response to Hurricanes Katrina and Rita: Audit of Food and Drug Administration's Award Process for a Contract With Cepheid (A-03-06-00542)
05-22-2007
Emergency Response to Hurricanes Katrina and Rita: Audit of Food and Drug Administration's Award Process for a Contract With Apple Hospitality Two LLC (A-03-06-00540)
02-15-2007
Food and Drug Administration's Resolution of Audit Recommendations (A-07-06-03083)
11-17-2006
Review of Corrective Actions Concerning the Human Subject Research Program

FY 2004

09-20-2004
Review of Food and Drug Administration's Bone Mass Study (A-03-03-00378)

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FY 2002

02-13-2002
Review of the Accuracy of the Food and Drug Administration's Official Establishment Inventory (A-15-01-20001)

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FY 2001

05-03-2001
Reporting Abuses of Persons with Disabilities (A-01-00-02502)

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FY 2000

12-14-1999
Review of the Food and Drug Administration's Handling of Adverse Drug Reaction Reports (A-15-98-50001)

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FY 1999

09-01-1999
Review of the Food and Drug Administration's Cost Increases for the Arkansas Regional Laboratory (A-15-98-50002)

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FY 1998

07-17-1998
Review of the Annual Reporting Process for Investigational New Drugs Regulated by the Food and Drug Administration's Center for Biologics Evaluation and Research (A-15-96-50001)
07-17-1998
Review of the Food and Drug Administration's Citizen Petition Process (A-15-97-50002)
03-02-1998
Review of the Food and Drug Administration's Internal Controls Over Its Purchase Card Activities (A-15-97-80002)

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FY 1997

06-04-1997
Review of the Food and Drug Administration's Inspection Process of Plasma Fractionators (A-03-97-00350)
05-16-1997
Review of the Food and Drug Administration's Handling of Issues Related to Conjugated Estrogens (A-15-96-50002)
05-05-1997
Compliance with the Prompt Payment Act by the Food and Drug Administration (A-15-96-40002)

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FY 1996

04-12-1996
Review of the Food and Drug Administration's Processing of 17 Error and Accident Reports Involving Blood (A-03-95-00350)
03-06-1996
Review of the Food and Drug Administration's Processes to Review Medical Device Submissions Under the Pre-Market Approval and Investigational Device Exemption Programs (A-15-95-50001)

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FY 1995

09-25-1995
Report on the Audit of the Food and Drug Administration's Revolving Fund for Certification and Other Services for Fiscal Year 1994 (A-17-94-00040)
09-25-1995
Report on the Audit of the Food and Drug Administration's Prescription Drug User Fee Account for Fiscal Year 1994 (A-17-95-00046)
08-02-1995
Review of the Food and Drug Administration's Processing of a New Drug Application for Therafectin (A-15-94-00023)
Reporting Process for Blood Establishments to Notify the Food and Drug Administration of Errors and Accidents Affecting Blood (A-03-93-00352)

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FY 1994

09-29-1994
Follow-up Review of Possible Improper Pre-Approval Promotion Activities (A-15-93-00018)

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FY 1993

08-27-1993
Financial Audit of the Food and Drug Administration's Revolving Fund for Certification and Other Services (A-15-93-00007)
06-07-1993
Review of the Food and Drug Administration's Headquarters Imprest Fund (A-15-92-00019)
02-26-1993
Follow-Up Review On Internal Control Weaknesses in the Food and Drug Administration's Medical Device 510(k) Review Process (A-03-92-00605)
10-26-1992
Follow-up Review of the Food and Drug Administration's Generic Drug Management Information System (A-15-91-00026)

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FY 1992

09-16-1992
Follow-Up Review of the Food and Drug Administration's Generic Drug Approval Process (A-15-91-00025)
08-06-1992
Review of Allegations of Mismanagement at the Food and Drug Administration - Newark District Office (A-02-91-02522)
02-21-1992
Audit of Issues Related to the Food and Drug Administration Review of Bovine Somatotropin (A-15-90-00046)

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