# Wyeth Lederle S.r.l – FDA Inspection, Apr 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/wyeth-lederle-srl/68b006c2-563c-4bdd-868c-dd5ef6220979
Source feed: FDA_Inspections

> FDA inspection 1012188 of Wyeth Lederle S.r.l, April 20, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 211. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1012188
- Company Name: Wyeth Lederle S.r.l
- Inspection Date: 2017-04-20
- 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: 4

## Related Documents

- FDA Inspection 1178127 - 2022-01-21
- [FDA Inspection 903600 - 2014-11-14](https://www.keypedia.com/records/fda_inspections/wyeth-lederle-srl/6eed9d57-b6d1-4bc4-a63b-2b3df655f1e2)
- [FDA Inspection 792624 - 2012-07-20](https://www.keypedia.com/records/fda_inspections/wyeth-lederle-srl/dc444967-e078-4b26-8b17-8010b6d7751b)
- FDA Inspection 637083 - 2009-12-04

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/david-j-gomes/dc3d1557-3bbc-4ed6-85fc-84b3462715c1)
- [FDA Associated Person](https://www.keypedia.com/people/junho-pak/4abe53fb-ad20-490d-9e71-6216a9f863f5)

Company: https://www.keypedia.com/companies/wyeth-lederle-srl/9fc09023-829f-4d59-be9b-44097f3d2fff

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