FDA Inspection
Neuromedex GmbHNeuromedex GmbH – FDA Inspection, Mar 21, 2024
Record Details
This FDA Inspection record concerns Neuromedex GmbH, with an inspection on March 21, 2024, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · 44115cf6-9fd2-4d20-909d-7e3379019ec9
Inspection Facts
- Inspection number
- 1235687
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.75(a)Lack of or inadequate process validation
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of Neuromedex GmbH
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 26, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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