FDA Inspection
G. Pohl-Boskamp GmbH & Co. KGG. Pohl-Boskamp GmbH & Co. KG – FDA Inspection, Feb 22, 2013
Record Details
This FDA Inspection record concerns G. Pohl-Boskamp GmbH & Co. KG, with an inspection on February 22, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- February 22, 2013
- Product Type
- Drugs
View Company Profile
ID · 12573127-b491-42f3-891c-31cd8f6f2620
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 826846
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.160(a)Following/documenting laboratory controls
- 21 CFR 211.192Investigations of discrepancies, failures
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Other FDA inspections of G. Pohl-Boskamp GmbH & Co. KG
6| Date | Classification | Office | Project area |
|---|---|---|---|
| September 14, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 28, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 15, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 11, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 3, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for G. Pohl-Boskamp GmbH & Co. KG
- FDA Inspection 1264909 - 2023-09-14
- FDA Inspection 1156166 - 2020-08-28
- FDA Inspection 1025477 - 2017-09-15
- FDA Inspection 957110 - 2016-02-11
- FDA Inspection 935101 - 2015-07-03
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