# Sanofi Winthrop Industrie – FDA Inspection, Jul 17, 2018

Source: https://www.keypedia.com/records/fda_inspections/sanofi-winthrop-industrie/27572d34-8446-4db8-8819-49ecbc085915
Source feed: FDA_Inspections

> FDA inspection 1063584 of Sanofi Winthrop Industrie, July 17, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063584
- Company Name: Sanofi Winthrop Industrie
- Inspection Date: 2018-07-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 1246180 - 2023-03-10
- FDA Inspection 1118089 - 2019-03-29
- [FDA Inspection 1022342 - 2017-07-25](https://www.keypedia.com/records/fda_inspections/sanofi-winthrop-industrie/cad42f47-1aad-4e97-912d-f854d2ceb564)
- FDA Inspection 998080 - 2016-09-14
- FDA Inspection 857683 - 2013-10-25

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/burnell-m-henry/dece4407-3597-4a58-8756-5abf9db43bbc)

Company: https://www.keypedia.com/companies/sanofi-winthrop-industrie/a9432693-ea49-48d8-941a-a91408c0acc4

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d
