FDA Inspection
AbbVie Deutschland GmbH & Co. KGAbbVie Deutschland GmbH & Co. KG – FDA Inspection, Oct 25, 2012
Record Details
This FDA Inspection record concerns AbbVie Deutschland GmbH & Co. KG, with an inspection on October 25, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- October 25, 2012
- Product Type
- Drugs
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ID · c17c30a4-104e-4c61-b34e-b5c14c99bc62
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 806316
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
- 21 CFR 211.192Extent of discrepancy, failure investigations
- 21 CFR 211.192Investigations of discrepancies, failures
- 21 CFR 211.67(b)Written procedures not established/followed
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Other FDA inspections of AbbVie Deutschland GmbH & Co. KG
7| Date | Classification | Office | Project area |
|---|---|---|---|
| May 16, 2025 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| September 28, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 19, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 23, 2017 | Not classified | Office of Inspections and Investigations | |
| September 18, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for AbbVie Deutschland GmbH & Co. KG
- FDA Inspection 1272781 - 2025-05-16
- FDA Inspection 1274472 - 2023-09-28
- FDA Inspection 1100574 - 2019-07-19
- FDA Inspection 1018744 - 2017-06-23
- FDA Inspection 900873 - 2014-09-18
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