FDA Inspection
Konapharma AGKonapharma AG – FDA Inspection, Jun 22, 2018
Record Details
This FDA Inspection record concerns Konapharma AG, with an inspection on June 22, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · fcc2ab15-1bae-4ee9-9ceb-c3d7c155af3c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1059703
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Konapharma AG
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 19, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 22, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 17, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 15, 2009 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Konapharma AG
- FDA Inspection 1257699 - 2024-06-19
- FDA Inspection 957960 - 2016-01-22
- FDA Inspection 827273 - 2013-04-17
- FDA Inspection 619086 - 2009-09-15
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