FDA Inspection
Mithra Pharmaceuticals Cdmo SAMithra Pharmaceuticals Cdmo SA – FDA Inspection, Jun 1, 2018
Record Details
This FDA Inspection record concerns Mithra Pharmaceuticals Cdmo SA, with an inspection on June 1, 2018, issued by the Office of Inspections and Investigations, covering human drugs.
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ID · 4b1ffefa-e62a-48a9-822f-0fdf95b48f5f
Inspection Facts
- Inspection number
- 1059221
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Mithra Pharmaceuticals Cdmo SA
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 2, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 2, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Mithra Pharmaceuticals Cdmo SA
- FDA Inspection 1228657 - 2022-12-02
- FDA Inspection 1064288 - 2018-08-02
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