FDA Inspection
Beaver-Visitec International, Inc.Beaver-Visitec International, Inc. – FDA Inspection, Mar 5, 2020
Record Details
This FDA Inspection record concerns Beaver-Visitec International, Inc., with an inspection on March 5, 2020, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 5, 2020
- Product Type
- Devices
View Company Profile
ID · 27f81141-9945-4d58-91f5-4c90fa7c29d8
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1123563
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
Other FDA inspections of Beaver-Visitec International, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 11, 2013 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| September 16, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 15, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Beaver-Visitec International, Inc.
- FDA Inspection 813386 - 2013-01-11
- FDA Inspection 746111 - 2011-09-16
- FDA Inspection 576023 - 2009-04-15
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