FDA Inspection
Teva Canada LimitedTeva Canada Limited – FDA Inspection, Nov 11, 2016
Record Details
This FDA Inspection record concerns Teva Canada Limited, with an inspection on November 11, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · c6845816-cd00-4a42-80f1-ff0261f534ae
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 996651
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Teva Canada Limited
5| Date | Classification | Office | Project area |
|---|---|---|---|
| November 3, 2023 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 31, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 14, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 9, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 27, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Teva Canada Limited
- FDA Inspection 1225068 - 2023-11-03
- FDA Inspection 1097611 - 2019-05-31
- FDA Inspection 865481 - 2014-02-14
- FDA Inspection 771387 - 2012-03-09
- FDA Inspection 566753 - 2009-02-27
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