FDA Inspection
RICARIMPEX SAS CO.RICARIMPEX SAS CO. – FDA Inspection, Sep 20, 2017
Record Details
This FDA Inspection record concerns RICARIMPEX SAS CO., with an inspection on September 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- Cynthia L. Aycock (Issuing Officer)
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ID · 23ada42f-abfb-4426-920a-0ed9005b66c8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1026687
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
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Other FDA inspections of RICARIMPEX SAS CO.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 28, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for RICARIMPEX SAS CO.
- FDA Inspection 1199963 - 2023-02-28
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