# BioLife Plasma Services L.P., Saint George, UT – FDA Inspections

Source: https://www.keypedia.com/companies/biolife-plasma-services-lp/2615e476-66b2-42fa-96c4-3506b035e306

> Inspection records and compliance data for BioLife Plasma Services L.P. in Saint George, Utah. 11 FDA inspections on record, last inspected February 26, 2026.

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## Details

- Name: BioLife Plasma Services L.P.
- FEI Number: 3006639569
- Address Line 1: 816 N 2860 E
- City: Saint George
- State: Utah
- Zip Code: 84790
- Country Name: United States
- Address: 816 N 2860 E, Saint George, Utah 84790, United States
- Country: United States

## Related Documents

- FDA Inspection 1305622 - BioLife Plasma Services L.P. - 2026-02-26 — classification: No Action Indicated (NAI), source: FDA, date: February 26, 2026
- FDA Inspection 1304010 - BioLife Plasma Services L.P. - 2026-02-17 — classification: No Action Indicated (NAI), source: FDA, date: February 17, 2026
- FDA Inspection 1301524 - BioLife Plasma Services L.P. - 2026-01-29 — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2026
- FDA Inspection 1283190 - BioLife Plasma Services L.P. - 2026-01-22 — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2026
- FDA Inspection 1299300 - BioLife Plasma Services L.P. - 2025-12-18 — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2025
- FDA Inspection 1298530 - BioLife Plasma Services L.P. - 2025-12-16 — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2025
- FDA Inspection 1292874 - BioLife Plasma Services L.P. - 2025-11-19 — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2025
- FDA Inspection 1208933 - BioLife Plasma Services L.P. - 2023-05-24 — classification: No Action Indicated (NAI), source: FDA, date: May 24, 2023
- FDA Inspection 1008596 - BioLife Plasma Services L.P. - 2017-03-28 — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2017
- FDA Inspection 830058 - BioLife Plasma Services L.P. - 2013-05-02 — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2013

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