FDA Inspection
Rhinosystems IncRhinosystems Inc – FDA Inspection, Feb 8, 2024
Record Details
This FDA Inspection record concerns Rhinosystems Inc, with an inspection on February 8, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · a16a3976-87b0-4693-bcdd-90c10a20f7b5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1228863
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of Rhinosystems Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 2, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 4, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Rhinosystems Inc
- FDA Inspection 996259 - 2016-12-02
- FDA Inspection 649782 - 2010-03-04
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