FDA Inspection
EthypharmEthypharm – FDA Inspection, Oct 19, 2012
Record Details
This FDA Inspection record concerns Ethypharm, with an inspection on October 19, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Ethypharm
- Inspection Date
- October 19, 2012
- Product Type
- Drugs
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ID · 2aa2318e-d41f-478c-b8ce-a9195892eb6b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 803055
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
1- 21 CFR 211.166(a)Lack of written stability program
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Other FDA inspections of Ethypharm
5| Date | Classification | Office | Project area |
|---|---|---|---|
| October 7, 2022 | VAI | Drug Quality Assurance | |
| November 5, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 26, 2018 | Not classified | Office of Inspections and Investigations | |
| December 5, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 19, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Ethypharm
- FDA Inspection 1301536 - 2022-10-07
- FDA Inspection 1181942 - 2020-11-05
- FDA Inspection 1042468 - 2018-01-26
- FDA Inspection 912110 - 2014-12-05
- FDA Inspection 573070 - 2009-02-19
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