FDA Inspection
Bionetek CorporationBionetek Corporation – FDA Inspection, Apr 10, 2012
Record Details
This FDA Inspection record concerns Bionetek Corporation, with an inspection on April 10, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Bionetek Corporation
- Inspection Date
- April 10, 2012
- Product Type
- Devices
View Company Profile
ID · bc735850-9ceb-41e2-9979-b14a2128ce42
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 776301
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Bionetek Corporation
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 27, 2011 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Bionetek Corporation
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.