FDA Inspection
Invivoscribe Technologies, Inc.Invivoscribe Technologies, Inc. – FDA Inspection, Sep 17, 2014
Record Details
This FDA Inspection record concerns Invivoscribe Technologies, Inc., with an inspection on September 17, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- September 17, 2014
- Product Type
- Devices
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ID · 5cfd25ac-0dc3-4789-986e-f00f4c9e33e4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 898383
- 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 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 |
| March 6, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 6, 2017 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Invivoscribe Technologies, Inc.
- FDA Inspection 1248327 - 2024-08-14
- FDA Inspection 1072296 - 2018-11-01
- FDA Inspection 1006006 - 2017-03-06
- FDA Inspection 1001718 - 2017-02-06
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