FDA Inspection
Innominata LLC, DBA GenbioInnominata LLC, DBA Genbio – FDA Inspection, Jun 13, 2014
Record Details
This FDA Inspection record concerns Innominata LLC, DBA Genbio, with an inspection on June 13, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Innominata LLC, DBA Genbio
- Inspection Date
- June 13, 2014
- Product Type
- Devices
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ID · c97434b4-7b18-48ed-b97d-8b9b5b7f1035
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 884197
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
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Other FDA inspections of Innominata LLC, DBA Genbio
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 26, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 25, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Innominata LLC, DBA Genbio
- FDA Inspection 1230350 - 2024-01-26
- FDA Inspection 1100372 - 2019-07-25
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