FDA Inspection
Biolife, LLCBiolife, LLC – FDA Inspection, Jul 31, 2009
Record Details
This FDA Inspection record concerns Biolife, LLC, with an inspection on July 31, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Biolife, LLC
- Inspection Date
- July 31, 2009
- Product Type
- Devices
View Company Profile
ID · d554a700-655a-4293-b098-f6a5ebeb6bce
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 599890
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Biolife, LLC
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 15, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 14, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 28, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 26, 2012 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 27, 2010 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Biolife, LLC
- FDA Inspection 1097262 - 2019-05-15
- FDA Inspection 1015370 - 2017-06-14
- FDA Inspection 838415 - 2013-06-28
- FDA Inspection 764655 - 2012-01-26
- FDA Inspection 677473 - 2010-08-27
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