FDA Inspection
Veran Medical Technologies IncVeran Medical Technologies Inc – FDA Inspection, Jan 31, 2019
Record Details
This FDA Inspection record concerns Veran Medical Technologies Inc, with an inspection on January 31, 2019, issued by the Center for Devices and Radiological Health, covering devices.
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ID · fb5486d8-99ca-4994-aea5-7db31ebd93ea
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1077815
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Veran Medical Technologies Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| February 23, 2023 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 29, 2021 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| February 23, 2018 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| February 4, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 25, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Veran Medical Technologies Inc
- FDA Inspection 1198214 - 2023-02-23
- FDA Inspection 1147930 - 2021-07-29
- FDA Inspection 1042301 - 2018-02-23
- FDA Inspection 912700 - 2015-02-04
- FDA Inspection 677305 - 2010-08-25
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