FDA Inspection
Bionix, LlcBionix, Llc – FDA Inspection, Jun 17, 2010
Record Details
This FDA Inspection record concerns Bionix, Llc, with an inspection on June 17, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Bionix, Llc
- Inspection Date
- June 17, 2010
- Product Type
- Devices
View Company Profile
ID · faa1ebf4-fd61-4631-aa83-f289f6f8e485
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 667265
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Bionix, Llc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| July 14, 2026 | VAI | Cincinnati District Office | Compliance: Devices |
| September 2, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 24, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 23, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 21, 2013 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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