FDA Inspection
Barr Laboratories, Inc. (subsidiary of Teva Pharmaceuticals)Barr Laboratories, Inc. (subsidiary of Teva Pharmaceuticals) – FDA Inspection, May 17, 2013
Record Details
This FDA Inspection record concerns Barr Laboratories, Inc. (subsidiary of Teva Pharmaceuticals), with an inspection on May 17, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- May 17, 2013
- Product Type
- Drugs
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ID · 03bd3030-a180-4674-a85e-de38fe3d4cef
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 832489
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.111Establishment of time limitations
- 21 CFR 211.67(b)Written procedures not established/followed
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Other FDA inspections of Barr Laboratories, Inc. (subsidiary of Teva Pharmaceuticals)
6| Date | Classification | Office | Project area |
|---|---|---|---|
| January 26, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 6, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 17, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 3, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 27, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Barr Laboratories, Inc. (subsidiary of Teva Pharmaceuticals)
- FDA Inspection 1001828 - 2017-01-26
- FDA Inspection 937325 - 2015-08-06
- FDA Inspection 888727 - 2014-07-17
- FDA Inspection 780103 - 2012-05-03
- FDA Inspection 732377 - 2011-06-27
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