FDA Inspection
Hevert Arzneimittel GmbH & Co. KGHevert Arzneimittel GmbH & Co. KG – FDA Inspection, Sep 29, 2017
Record Details
This FDA Inspection record concerns Hevert Arzneimittel GmbH & Co. KG, with an inspection on September 29, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · a3952b4e-99f2-4c71-bf6a-b1b6d47ba0ff
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1026975
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
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Other FDA inspections of Hevert Arzneimittel GmbH & Co. KG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 6, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 12, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Hevert Arzneimittel GmbH & Co. KG
- FDA Inspection 1276837 - 2022-12-06
- FDA Inspection 1127151 - 2020-03-12
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