# BioLife Plasma Services, L.P. - Inspection Records

Source: https://www.keypedia.com/companies/biolife-plasma-services-lp/7acf14da-ec3d-4afb-a917-c97602058b0e

> Inspection records and compliance data for BioLife Plasma Services, L.P. in Denton, Texas. Access full analysis and detailed observations.

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## Details

- Name: BioLife Plasma Services, L.P.
- FEI Number: 1627981
- City: Denton
- State: Texas
- Country Name: United States
- Address Line 1: 3455 Quail Creek Dr
- Zip Code: 76208

## Related Documents

- [FDA Inspection 1153743 - BioLife Plasma Services, L.P. - 2021-09-23](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/c8086fd9-4584-4d21-a187-1edea4d65da5) — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2021
- [FDA Inspection 1153743 - BioLife Plasma Services, L.P. - 2021-09-23](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/c90dc1e2-18e3-45df-9924-79506346c1e1) — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2021
- [FDA Inspection 1038349 - BioLife Plasma Services, L.P. - 2018-01-10](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/6f621d93-5c08-45b7-866d-277978eedc4c) — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2018
- [FDA Inspection 945062 - BioLife Plasma Services, L.P. - 2015-10-08](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/c9267882-a610-4700-8edc-c73f16baa0cd) — classification: No Action Indicated (NAI), source: FDA, date: October 8, 2015
- [FDA Inspection 844418 - BioLife Plasma Services, L.P. - 2013-08-09](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/eab3dff3-e958-4073-aea3-1fb0ac572f70) — classification: No Action Indicated (NAI), source: FDA, date: August 9, 2013
- [FDA Inspection 706154 - BioLife Plasma Services, L.P. - 2011-01-18](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/44931fa4-2f6c-40d0-96b1-f146e2ead743) — classification: No Action Indicated (NAI), source: FDA, date: January 18, 2011

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