FDA Inspection
Dreve Otoplastik GmbhDreve Otoplastik Gmbh – FDA Inspection, Sep 7, 2017
Record Details
This FDA Inspection record concerns Dreve Otoplastik Gmbh, with an inspection on September 7, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
- Person
- Rita K. Vick (Issuing Officer)
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ID · faeaed01-6283-4510-81d0-b5f2c7514f0c
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 1027670
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Dreve Otoplastik Gmbh
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 21, 2014 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
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