FDA Inspection
Venni Instruments IncVenni Instruments Inc – FDA Inspection, Dec 13, 2012
Record Details
This FDA Inspection record concerns Venni Instruments Inc, with an inspection on December 13, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Venni Instruments Inc
- Inspection Date
- December 13, 2012
- Product Type
- Devices
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ID · 86760eca-09aa-4b8c-ab90-16ef3195c9be
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 810371
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of Venni Instruments Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 17, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 31, 2015 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Venni Instruments Inc
- FDA Inspection 1038015 - 2018-01-17
- FDA Inspection 920978 - 2015-03-31
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