FDA Inspection
COULOT DECOLLETAGECOULOT DECOLLETAGE – FDA Inspection, Sep 13, 2013
Record Details
This FDA Inspection record concerns COULOT DECOLLETAGE, with an inspection on September 13, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- COULOT DECOLLETAGE
- Inspection Date
- September 13, 2013
- Product Type
- Devices
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ID · 7ea05ae5-c76e-4d9d-b7b4-e581ce35a03d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 852627
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Complaints
- 21 CFR 820.100(b)Documentation
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Other FDA inspections of COULOT DECOLLETAGE
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 3, 2026 | Not classified | Office of Inspections and Investigations | |
| April 5, 2024 | Not classified | Office of Inspections and Investigations | |
| October 19, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for COULOT DECOLLETAGE
- FDA Inspection 1326468 - 2026-06-03
- FDA Inspection 1236345 - 2024-04-05
- FDA Inspection 994508 - 2016-10-19
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