FDA Inspection
Viatris Inc.Viatris Inc. – FDA Inspection, Feb 17, 2010
Record Details
This FDA Inspection record concerns Viatris Inc., with an inspection on February 17, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Viatris Inc.
- Inspection Date
- February 17, 2010
- Product Type
- Drugs
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ID · f5f6fe8c-7135-4a21-a5b5-b829c9c44dbd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 649431
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.188(b)(11)Identification of persons involved, each significant step
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of Viatris Inc.
21| Date | Classification | Office | Project area |
|---|---|---|---|
| August 28, 2026 | Not classified | Baltimore District Office | |
| April 28, 2026 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 18, 2023 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| May 26, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 15, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Viatris Inc.
- FDA Inspection 1302530 - 2026-08-28
- FDA Inspection 1311680 - 2026-04-28
- FDA Inspection 1219018 - 2023-08-18
- FDA Inspection 1170444 - 2022-05-26
- FDA Inspection 1099590 - 2019-08-15
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