FDA Inspection
G. Pohl-Boskamp GmbH & Co. KGG. Pohl-Boskamp GmbH & Co. KG – FDA Inspection, Nov 5, 2010
Record Details
This FDA Inspection record concerns G. Pohl-Boskamp GmbH & Co. KG, with an inspection on November 5, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- November 5, 2010
- Product Type
- Drugs
View Company Profile
ID · fc0018e0-8e79-4700-b825-294a9be200b0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 700757
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.100(b)Procedure Deviations Recorded and Justified
- 21 CFR 211.198(a)Complaint Handling Procedure
- 21 CFR 211.68(a)Written calibration / inspection records not kept
- 21 CFR 211.192Written record of investigation incomplete
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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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