# BioLife Plasma Services Lp - Inspection Records

Source: https://www.keypedia.com/companies/biolife-plasma-services-lp/0ad77a19-e777-4523-8295-9c3305b5ad25

> Inspection records and compliance data for BioLife Plasma Services Lp in Hoover, Alabama. Access full analysis and detailed observations.

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## Details

- Name: BioLife Plasma Services Lp
- FEI Number: 1000221914
- City: Hoover
- State: Alabama
- Country Name: United States
- Address Line 1: 2197 Parkway Lake Dr
- Zip Code: 35244

## Related Documents

- [FDA Inspection 1058472 - BioLife Plasma Services Lp - 2018-06-07](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/3455d5d9-7929-4f33-a8ae-ff3945c5bf25) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2018
- [FDA Inspection 969922 - BioLife Plasma Services Lp - 2016-05-05](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/a475a863-fae1-4ab3-9509-9929ea8c0e37) — classification: No Action Indicated (NAI), source: FDA, date: May 5, 2016
- [FDA Inspection 873574 - BioLife Plasma Services Lp - 2014-04-03](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/73e427af-8fa5-4224-96c1-616d94de3716) — classification: No Action Indicated (NAI), source: FDA, date: April 3, 2014
- [FDA Inspection 810503 - BioLife Plasma Services Lp - 2012-12-10](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/c96f73c4-1fc7-438e-9938-79d2fe019893) — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2012
- [FDA Inspection 743402 - BioLife Plasma Services Lp - 2011-08-04](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/cc73f8aa-d331-468c-9e9b-ce4c6d0e75ae) — classification: No Action Indicated (NAI), source: FDA, date: August 4, 2011
- [FDA Inspection 574591 - BioLife Plasma Services Lp - 2009-04-09](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/d3b6b6c0-edef-492c-965e-223cce5c1bb6) — classification: No Action Indicated (NAI), source: FDA, date: April 9, 2009

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