# EuroAPI UK Limited – FDA Inspection, Mar 6, 2017

Source: https://www.keypedia.com/records/fda_inspections/euroapi-uk-limited/61587209-2192-4679-ade3-833b100a670f
Source feed: FDA_Inspections

> FDA inspection 1012443 of EuroAPI UK Limited, March 06, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1012443
- Company Name: EuroAPI UK Limited
- Inspection Date: 2017-03-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

- 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

## Related Officers

- [Russell J. Glapion](https://www.keypedia.com/people/russell-j-glapion/54dd6274-563a-44fe-8016-2ebd700be7a0)

Company: https://www.keypedia.com/companies/euroapi-uk-limited/8471d752-7ba8-4884-891b-c77bf6e3da2b

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c