FDA Inspection
Clariance-SASClariance-SAS – FDA Inspection, Jan 29, 2015
Record Details
This FDA Inspection record concerns Clariance-SAS, with an inspection on January 29, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Clariance-SAS
- Inspection Date
- January 29, 2015
- Product Type
- Devices
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ID · f753eebc-9d00-4fa5-ae64-9026abeb9ad3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 916297
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.100(b)Documentation
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Clariance-SAS
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 26, 2024 | VAI | Office of Inspections and Investigations | Compliance: Medical Devices |
| June 14, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Clariance-SAS
- FDA Inspection 1250090 - 2024-09-26
- FDA Inspection 1062738 - 2018-06-14
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