FDA Inspection
Incisive,Inc.Incisive,Inc. – FDA Inspection, Jun 21, 2012
Record Details
This FDA Inspection record concerns Incisive,Inc., with an inspection on June 21, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Incisive,Inc.
- Inspection Date
- June 21, 2012
- Product Type
- Devices
View Company Profile
ID · 6b70db64-0078-42cb-af01-0bbf314be216
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 787435
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Incisive,Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 11, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 23, 2017 | Not classified | San Francisco District Office | |
| September 14, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Incisive,Inc.
- FDA Inspection 1037948 - 2018-01-11
- FDA Inspection 1029894 - 2017-08-23
- FDA Inspection 618028 - 2009-09-14
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