FDA Inspection
DFS Diamon GmbHDFS Diamon GmbH – FDA Inspection, Sep 20, 2019
Record Details
This FDA Inspection record concerns DFS Diamon GmbH, with an inspection on September 20, 2019, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · 0980e02e-8879-47a4-9efa-57322dab3d5b
Inspection Facts
- Inspection number
- 1102433
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.184DHR content
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.50(a)(1)Evaluation and Selection, Suppliers, Contractors, etc.
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