FDA Inspection
Bioserv CorporationBioserv Corporation – FDA Inspection, Jul 31, 2017
Record Details
This FDA Inspection record concerns Bioserv Corporation, with an inspection on July 31, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · cc62ac96-b17a-4005-bd7c-fa7981de2d9c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1022355
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Bioserv Corporation
6| Date | Classification | Office | Project area |
|---|---|---|---|
| January 12, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 23, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 24, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 7, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 12, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Bioserv Corporation
- FDA Inspection 1195989 - 2023-01-12
- FDA Inspection 863803 - 2014-01-23
- FDA Inspection 804269 - 2012-10-24
- FDA Inspection 756094 - 2011-12-07
- FDA Inspection 656899 - 2010-04-12
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