# Siegfried (St. Vulbas) SAS, Saint-Vulbas, France – FDA Inspections

Source: https://www.keypedia.com/companies/siegfried-st-vulbas-sas/cc817d89-99cd-49e7-b4a0-b87ebed9ecb6

> Inspection records and compliance data for Siegfried (St. Vulbas) SAS in Saint-Vulbas. 6 FDA inspections on record, 1 Form 483, last inspected January 13, 2023.

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## Details

- Name: Siegfried (St. Vulbas) SAS
- FEI Number: 3002807787
- Business Operations: API MANUFACTURE
- Address Line 1: Parc Industriel De La Plaine De L Ain, 530 Allee De La Luye
- City: Saint-Vulbas
- Country Name: France
- Address: Parc Industriel De La Plaine De L Ain, 530 Allee De La Luye, Saint-Vulbas, France
- Country: France

## Related Documents

- [FDA Inspection 1247255 - Siegfried (St. Vulbas) SAS - 2023-01-13](https://www.keypedia.com/records/fda_inspections/siegfried-st-vulbas-sas/25121383-0606-4877-903d-a0d564e04013) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2023
- FDA Inspection 1125537 - Siegfried (St. Vulbas) SAS - 2019-11-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 7, 2019
- [FDA Inspection 1063219 - Siegfried (St. Vulbas) SAS - 2018-06-29](https://www.keypedia.com/records/fda_inspections/siegfried-st-vulbas-sas/7e4ce7d7-614d-43bc-961a-191b332336ec) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2018
- [FDA Inspection 990166 - Siegfried (St. Vulbas) SAS - 2016-09-23](https://www.keypedia.com/records/fda_inspections/siegfried-st-vulbas-sas/96026e0b-8591-41bc-956f-a11d10d5f804) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 23, 2016
- [FDA Inspection 889637 - Siegfried (St. Vulbas) SAS - 2013-12-18](https://www.keypedia.com/records/fda_inspections/siegfried-st-vulbas-sas/64af6656-5581-41ee-b2c6-8d577d4607c4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 18, 2013
- FDA Inspection 645432 - Siegfried (St. Vulbas) SAS - 2010-01-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 22, 2010

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