FDA Inspection
Corden Pharma ChenoveCorden Pharma Chenove – FDA Inspection, Sep 13, 2019
Record Details
This FDA Inspection record concerns Corden Pharma Chenove, with an inspection on September 13, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · bb23f210-45cc-4af8-865c-3dca9316d9e6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1101908
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Corden Pharma Chenove
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 14, 2025 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 26, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 14, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 20, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Corden Pharma Chenove
- FDA Inspection 1277830 - 2025-02-14
- FDA Inspection 988106 - 2016-08-26
- FDA Inspection 874552 - 2014-03-14
- FDA Inspection 633571 - 2009-11-20
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