FDA Inspection
Kessel Medintim GmbhKessel Medintim Gmbh – FDA Inspection, Nov 2, 2017
Record Details
This FDA Inspection record concerns Kessel Medintim Gmbh, with an inspection on November 2, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Person
- Seema S. Singh (Issuing Officer)
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ID · 9d4bd2ea-5bff-46d9-afe5-6eefe6914bbd
Inspection Facts
- Inspection number
- 1030511
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.30(f)Design verification - output does not meet input requirement
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