FDA Inspection
EuroAPI UK LimitedEuroAPI UK Limited – FDA Inspection, Mar 6, 2017
Record Details
This FDA Inspection record concerns EuroAPI UK Limited, with an inspection on March 6, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 61587209-2192-4679-ade3-833b100a670f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1012443
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of EuroAPI UK Limited
5| Date | Classification | Office | Project area |
|---|---|---|---|
| November 3, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 22, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 27, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 13, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 13, 2008 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for EuroAPI UK Limited
- FDA Inspection 1238555 - 2022-11-03
- FDA Inspection 1155931 - 2019-07-22
- FDA Inspection 919149 - 2015-02-27
- FDA Inspection 720237 - 2011-04-13
- FDA Inspection 551802 - 2008-11-13
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