FDA Inspection
EthypharmEthypharm – FDA Inspection, Sep 13, 2012
Record Details
This FDA Inspection record concerns Ethypharm, with an inspection on September 13, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Ethypharm
- Inspection Date
- September 13, 2012
- Product Type
- Drugs
View Company Profile
ID · 773d51dc-a598-4b17-b8b4-118b9ce5505a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 814715
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Ethypharm
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 25, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 22, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 12, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 23, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Ethypharm
- FDA Inspection 1206209 - 2023-03-25
- FDA Inspection 1085912 - 2018-02-22
- FDA Inspection 912183 - 2014-12-12
- FDA Inspection 573367 - 2009-02-23
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