# BioLife Plasma Services LP - Inspection Records

Source: https://www.keypedia.com/companies/biolife-plasma-services-lp/90e7e19d-af30-439d-a241-210489ba21af

> Inspection records and compliance data for BioLife Plasma Services LP in Moorhead, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: BioLife Plasma Services LP
- FEI Number: 3006769911
- City: Moorhead
- State: Minnesota
- Country Name: United States
- Address Line 1: 2960 12th St S
- Zip Code: 56560

## Related Documents

- [FDA Inspection 1211185 - BioLife Plasma Services LP - 2023-06-29](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/ac218e59-20e8-477a-8948-5874ef2b0bcb) — classification: No Action Indicated (NAI), source: FDA, date: June 29, 2023
- [FDA Inspection 1018617 - BioLife Plasma Services LP - 2017-06-07](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/8aeed408-987a-4848-b2e6-8f520b9edf0f) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2017
- [FDA Inspection 945442 - BioLife Plasma Services LP - 2015-09-02](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/997cdd17-00f4-4046-8199-6052ca6aaaa5) — classification: No Action Indicated (NAI), source: FDA, date: September 2, 2015
- [FDA Inspection 849344 - BioLife Plasma Services LP - 2013-09-20](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/6dcfc146-3f94-42df-9f9a-d4d368f1756c) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2013
- [FDA Inspection 746370 - BioLife Plasma Services LP - 2011-09-23](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/2d3edfc6-e001-42c7-91d0-b34226bf35a3) — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2011
- [FDA Inspection 683983 - BioLife Plasma Services LP - 2010-09-17](https://www.keypedia.com/records/fda_inspections/biolife-plasma-services-lp/e5f08fa7-ccbf-4bc8-bcee-78f4334dfd13) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2010

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