# Biolife, LLC – FDA Inspection, Jul 31, 2009

Source: https://www.keypedia.com/records/fda_inspections/biolife-llc/d554a700-655a-4293-b098-f6a5ebeb6bce
Source feed: FDA_Inspections

> FDA inspection 599890 of Biolife, LLC, July 31, 2009. Classification: Voluntary Action Indicated (VAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 599890
- Company Name: Biolife, LLC
- Inspection Date: 2009-07-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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- [FDA Inspection 1015370 - 2017-06-14](https://www.keypedia.com/records/fda_inspections/biolife-llc/c3898726-c1dd-4061-9ca3-6a2a5dc26ab7)
- [FDA Inspection 838415 - 2013-06-28](https://www.keypedia.com/records/fda_inspections/biolife-llc/e9b0c363-befd-4ab6-a516-de6596e10ae9)
- [FDA Inspection 764655 - 2012-01-26](https://www.keypedia.com/records/fda_inspections/biolife-llc/ee60e292-568b-45f5-897c-57fd0d127ad1)
- [FDA Inspection 677473 - 2010-08-27](https://www.keypedia.com/records/fda_inspections/biolife-llc/6f99047c-cbd9-47c8-adfb-5f750b923836)

Company: https://www.keypedia.com/companies/biolife-llc/ff5d8406-ab0e-4f14-9099-0c4c11848659

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7