FDA Inspection
Excella GmbH & Co. KGExcella GmbH & Co. KG – FDA Inspection, Jul 12, 2019
Record Details
This FDA Inspection record concerns Excella GmbH & Co. KG, with an inspection on July 12, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 4ac3f0b8-7ffe-4ca8-847d-71a06c7ee0ce
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1098271
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Excella GmbH & Co. KG
7| Date | Classification | Office | Project area |
|---|---|---|---|
| October 19, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 10, 2018 | Not classified | Office of Inspections and Investigations | |
| March 17, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 29, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 17, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Excella GmbH & Co. KG
- FDA Inspection 1205496 - 2022-10-19
- FDA Inspection 1064238 - 2018-08-10
- FDA Inspection 1012240 - 2017-03-17
- FDA Inspection 933855 - 2015-05-29
- FDA Inspection 831974 - 2013-05-17
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