FDA Inspection
Venni Instruments IncVenni Instruments Inc – FDA Inspection, Jan 17, 2018
Record Details
This FDA Inspection record concerns Venni Instruments Inc, with an inspection on January 17, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · fe680c97-4eec-4692-909e-0321507460e9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1038015
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.198(e)Records of complaint investigation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Venni Instruments Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 31, 2015 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| December 13, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Venni Instruments Inc
- FDA Inspection 920978 - 2015-03-31
- FDA Inspection 810371 - 2012-12-13
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