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U.S. Department of Health and Human Services

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Number of highest risk domestic inspections in the month resulting in a classification of Official Action Indicated (OAI)

Dictionary: The number of high-risk product inspections where objectionable conditions were found and a regulatory action is recommended are classified as an Official Action Indicated. This includes voluntary recalls initiated by the firm, or FDA requested recalls when the firm is hesitant to conduct a voluntary recall.

Fiscal Year - 2012

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TimeTargetNumber Classified as OAI
Oct 2011N/A31
Nov 2011N/A40
Dec 2011N/A42
Jan 2012N/A35
Feb 2012N/A41
Mar 2012N/A48
Apr 2012N/A32
May 2012N/A51
Jun 2012N/A69
Jul 2012N/A57
Aug 2012N/A71
Sep 2012N/A62

FY 2012 Total: 579

Percent of highest risk domestic inspections in the month resulting in a classification of Official Action Indicated

Fiscal Year - 2012
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TimeTargetPercent Classified as OAI
Oct 2011N/A3
Nov 2011N/A3
Dec 2011N/A3
Jan 2012N/A3
Feb 2012N/A3
Mar 2012N/A3
Apr 2012N/A3
May 2012N/A4
Jun 2012N/A6
Jul 2012N/A6
Aug 2012N/A7
Sep 2012N/A7

Glossary

Note: The data provided on this website is produced on an ongoing basis for performance management purposes and is subject to change due to updates of preliminary estimates, corrections, or other reasons. In addition, FDA may change the type or amount of data provided on this website at any time. Information marked as "Completed" may include measures and/or key projects for which activities are ongoing but no longer tracked as part of FDA-TRACK.