FDA Inspection
Sever Pharma SolutionsSever Pharma Solutions – FDA Inspection, Dec 15, 2017
Record Details
This FDA Inspection record concerns Sever Pharma Solutions, with an inspection on December 15, 2017, issued by the Office of Inspections and Investigations, covering human drugs.
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ID · d7d3fde0-67e8-4e7e-b7c9-3a75ae89a2e4
Inspection Facts
- Inspection number
- 1036638
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Sever Pharma Solutions
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 12, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 31, 2023 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 23, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 1, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 27, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Sever Pharma Solutions
- FDA Inspection 1268673 - 2023-05-12
- FDA Inspection 1204531 - 2023-03-31
- FDA Inspection 1093984 - 2017-11-23
- FDA Inspection 973494 - 2016-06-01
- FDA Inspection 871578 - 2014-03-27
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