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FDA Inspection
•Biolife, LLC•January 26, 2012

Biolife, LLC – FDA Inspection, Jan 26, 2012

Record Details

This FDA Inspection record concerns Biolife, LLC, with an inspection on January 26, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company
Biolife, LLC
Inspection Date
January 26, 2012
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · ee60e292-568b-45f5-897c-57fd0d127ad1

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
764655
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Biolife, LLC

5
DateClassificationOfficeProject area
May 15, 2019NAICenter for Devices and Radiological HealthCompliance: Devices
June 14, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
June 28, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
August 27, 2010OAICenter for Devices and Radiological HealthCompliance: Devices
July 31, 2009VAICenter for Devices and Radiological HealthCompliance: 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 677473 - 2010-08-27
  • FDA Inspection 599890 - 2009-07-31

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