FDA Inspection
Synthesia, a.s.Synthesia, a.s. – FDA Inspection, May 16, 2014
Record Details
This FDA Inspection record concerns Synthesia, a.s., with an inspection on May 16, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Synthesia, a.s.
- Inspection Date
- May 16, 2014
- Product Type
- Drugs
View Company Profile
ID · d8c740fe-ac34-43bb-b4c1-83b663a7c59b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 879003
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Synthesia, a.s.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 18, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 29, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 18, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 31, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Synthesia, a.s.
- FDA Inspection 1271689 - 2023-01-18
- FDA Inspection 1123598 - 2019-05-29
- FDA Inspection 954063 - 2015-12-18
- FDA Inspection 735366 - 2011-03-31
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