# BioLife Plasma Services L.P. - Inspection Records

Source: https://www.keypedia.com/companies/biolife-plasma-services-lp/18916c89-9667-4970-a77a-bd9fe1c1c043

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

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## Details

- Name: BioLife Plasma Services L.P.
- FEI Number: 1000116800
- City: Fargo
- State: North Dakota
- Country Name: United States
- Address Line 1: 2617 12th Ave S
- Zip Code: 58103

## Related Documents

- [FDA Inspection 1150498 - BioLife Plasma Services L.P. - 2021-08-16](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/b70fab74-a27c-4fe1-b440-8fd890dbd1ff) — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2021
- [FDA Inspection 1150498 - BioLife Plasma Services L.P. - 2021-08-16](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/d67d303d-df6a-48d5-95e3-444b2093025a) — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2021
- [FDA Inspection 1018618 - BioLife Plasma Services L.P. - 2017-06-09](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/459e862a-4994-4f9d-89b6-2fc0a76e8568) — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2017
- [FDA Inspection 896593 - BioLife Plasma Services L.P. - 2014-09-25](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/6ce98e86-dfda-4098-8392-2569ef13a5c8) — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2014
- [FDA Inspection 758662 - BioLife Plasma Services L.P. - 2011-12-15](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/c880b9bd-fbae-45c0-af43-3dd8f821468f) — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2011
- [FDA Inspection 678413 - BioLife Plasma Services L.P. - 2010-08-26](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/73ea277b-a729-4ebf-bc79-003b4f26aa8f) — classification: No Action Indicated (NAI), source: FDA, date: August 26, 2010

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