FDA Inspection
Siegfried (St. Vulbas) SASSiegfried (St. Vulbas) SAS – FDA Inspection, Dec 18, 2013
Record Details
This FDA Inspection record concerns Siegfried (St. Vulbas) SAS, with an inspection on December 18, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Siegfried (St. Vulbas) SAS
- Inspection Date
- December 18, 2013
- Product Type
- Drugs
View Company Profile
ID · 64af6656-5581-41ee-b2c6-8d577d4607c4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 889637
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
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 |
| June 29, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 23, 2016 | 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 1063219 - 2018-06-29
- FDA Inspection 990166 - 2016-09-23
- FDA Inspection 645432 - 2010-01-22
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