FDA Inspection
Siegfried (St. Vulbas) SASSiegfried (St. Vulbas) SAS – FDA Inspection, Jun 29, 2018
Record Details
This FDA Inspection record concerns Siegfried (St. Vulbas) SAS, with an inspection on June 29, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
- Person
- Yumi J. Hiramine (Issuing Officer)
View Company Profile
ID · 7e4ce7d7-614d-43bc-961a-191b332336ec
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1063219
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Siegfried (St. Vulbas) SAS
5| Date | Classification | Office | Project area |
|---|---|---|---|
| January 13, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 7, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 23, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 18, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 22, 2010 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Siegfried (St. Vulbas) SAS
- FDA Inspection 1247255 - 2023-01-13
- FDA Inspection 1125537 - 2019-11-07
- FDA Inspection 990166 - 2016-09-23
- FDA Inspection 889637 - 2013-12-18
- FDA Inspection 645432 - 2010-01-22
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