FDA Inspection
Taro Pharmaceuticals Inc.Taro Pharmaceuticals Inc. – FDA Inspection, Jan 20, 2017
Record Details
This FDA Inspection record concerns Taro Pharmaceuticals Inc., with an inspection on January 20, 2017, issued by the Office of Inspections and Investigations, covering human drugs.
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ID · 03164ddc-43fe-4ffd-90c6-1c18d24b8d7d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1001628
- FDA center
- Human Drugs
- Project area
- Generic Drug Evaluation
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 211.103Actual vs. theoretical yields not determined
- 21 CFR 211.42(c)(10)(i)Floors, walls, ceiling surfaces
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Other FDA inspections of Taro Pharmaceuticals Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| March 27, 2026 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 20, 2024 | Not classified | Office of Inspections and Investigations | |
| September 16, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 3, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 29, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Taro Pharmaceuticals Inc.
- FDA Inspection 1312804 - 2026-03-27
- FDA Inspection 1257703 - 2024-09-20
- FDA Inspection 1180887 - 2022-09-16
- FDA Inspection 1088553 - 2019-05-03
- FDA Inspection 984831 - 2016-07-29
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