# BioLife Plasma Services L.P. - Inspection Records

Source: https://www.keypedia.com/companies/biolife-plasma-services-lp/a7a7b7fc-d052-4aca-ab3c-362ff27ee65d

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

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## Details

- Name: BioLife Plasma Services L.P.
- FEI Number: 1045838
- City: Greensboro
- State: North Carolina
- Country Name: United States
- Address Line 1: 1409 Yanceyville St Ste A
- Zip Code: 27405

## Related Documents

- [FDA Inspection 1129849 - BioLife Plasma Services L.P. - 2020-08-31](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/9dd6114e-dac5-43d7-9212-f38db08da9d6) — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2020
- [FDA Inspection 1129849 - BioLife Plasma Services L.P. - 2020-08-31](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/09ab6bbf-767e-4926-b66d-12e9414e84a3) — classification: No Action Indicated (NAI), source: FDA, date: August 31, 2020
- [FDA Inspection 1032341 - BioLife Plasma Services L.P. - 2017-11-09](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/8a7ac6e9-aeff-459e-9a8d-2649f83dc6f8) — classification: No Action Indicated (NAI), source: FDA, date: November 9, 2017
- [FDA Inspection 894891 - BioLife Plasma Services L.P. - 2014-09-04](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/cbccfdac-bbd5-4fac-ae47-62fa08388c34) — classification: No Action Indicated (NAI), source: FDA, date: September 4, 2014
- [FDA Inspection 789975 - BioLife Plasma Services L.P. - 2012-06-07](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/f50f371a-a6c8-42ac-bcc3-456377d80982) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2012
- [FDA Inspection 658722 - BioLife Plasma Services L.P. - 2010-04-22](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/4c786cd3-a938-4b9d-ae39-0f383f6f31cc) — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2010

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