FDA Inspection
Baxter Deutschland GmbHBaxter Deutschland GmbH – FDA Inspection, May 28, 2025
Record Details
This FDA Inspection record concerns Baxter Deutschland GmbH, with an inspection on May 28, 2025, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · ab2bc592-2030-4c1b-9bea-829ff0a34dbd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1288760
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Baxter Deutschland GmbH
4| Date | Classification | Office | Project area |
|---|---|---|---|
| November 11, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 14, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 22, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 26, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Baxter Deutschland GmbH
- FDA Inspection 1193847 - 2022-11-11
- FDA Inspection 1060487 - 2018-06-14
- FDA Inspection 957912 - 2016-01-22
- FDA Inspection 746997 - 2011-08-26
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