FDA Inspection
MEDTECH SASMEDTECH SAS – FDA Inspection, Jul 24, 2025
Record Details
This FDA Inspection record concerns MEDTECH SAS, with an inspection on July 24, 2025, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · b6b95133-b762-4616-99be-8a1e88dd629e
Inspection Facts
- Inspection number
- 1275015
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Medical Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 803.52(a)(1)Patient Name or Other Identifier
- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
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Other FDA inspections of MEDTECH SAS
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 16, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for MEDTECH SAS
- FDA Inspection 1038442 - 2017-11-16
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