FDA Inspection
Clariance-SASClariance-SAS – FDA Inspection, Sep 26, 2024
Record Details
This FDA Inspection record concerns Clariance-SAS, with an inspection on September 26, 2024, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · 9cbeb5dd-483e-420c-a772-2c44be98694b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1250090
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Medical Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.100(b)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Clariance-SAS
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 14, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 29, 2015 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Clariance-SAS
- FDA Inspection 1062738 - 2018-06-14
- FDA Inspection 916297 - 2015-01-29
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