FDA Inspection
Invivoscribe Technologies, Inc.Invivoscribe Technologies, Inc. – FDA Inspection, Mar 6, 2017
Record Details
This FDA Inspection record concerns Invivoscribe Technologies, Inc., with an inspection on March 6, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- People
- Freddy D. Tita-Nwa (Issuing Officer)
- Scott K. Zika (Issuing Officer)
- Theresa Kirkham
View Company Profile
ID · f7a4ebdc-e397-43d7-85cc-ad14c07c912f
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1006006
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Invivoscribe Technologies, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 14, 2024 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 1, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 6, 2017 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| September 17, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Invivoscribe Technologies, Inc.
- FDA Inspection 1248327 - 2024-08-14
- FDA Inspection 1072296 - 2018-11-01
- FDA Inspection 1001718 - 2017-02-06
- FDA Inspection 898383 - 2014-09-17
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