FDA Inspection
Medidenta International IncMedidenta International Inc – FDA Inspection, Nov 5, 2025
Record Details
This FDA Inspection record concerns Medidenta International Inc, with an inspection on November 5, 2025, issued by the San Francisco District Office, covering medical devices & rad health.
- Company
- Medidenta International Inc
- Inspection Date
- November 5, 2025
- Product Type
- Medical Devices & Rad Health
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ID · 9bfa147a-439a-44aa-adfb-2a763c25d8f1
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1290392
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Medical Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.200(a)Servicing - Lack of or inadequate procedures
- 21 CFR 820.184Lack of or inadequate DHR procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Medidenta International Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 17, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 11, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medidenta International Inc
- FDA Inspection 942743 - 2015-09-17
- FDA Inspection 739666 - 2011-08-11
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