# BioLife Plasma Services L.P. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/biolife-plasma-services-lp/5e27f616-8372-4259-b857-5884a70f2a5e

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

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## Details

- Name: BioLife Plasma Services L.P.
- FEI Number: 3007326193
- City: Elkhart
- State: Indiana
- Country Name: United States
- Address Line 1: 2715 Emerson Dr
- Zip Code: 46514

## Related Documents

- [FDA Inspection 1277863 - BioLife Plasma Services L.P. - 2025-07-24](https://www.globalkeysolutions.net/records/fda_inspections/biolife-plasma-services-lp/0a0faef1-e90b-435f-b1e5-b310e397f006) — source: FDA, date: July 24, 2025
- [FDA Inspection 1277863 - BioLife Plasma Services L.P. - 2025-07-24](https://www.globalkeysolutions.net/records/fda_inspections/biolife-plasma-services-lp/d1fdb0e7-a05d-4fa0-95d1-8b86a878ce47) — classification: No Action Indicated (NAI), source: FDA, date: July 24, 2025
- [FDA Inspection 1028517 - BioLife Plasma Services L.P. - 2017-09-27](https://www.globalkeysolutions.net/records/fda_inspections/biolife-plasma-services-lp/9fbbcfaa-ef45-4d2a-b53d-0df0b9c384ae) — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2017
- [FDA Inspection 890444 - BioLife Plasma Services L.P. - 2014-08-13](https://www.globalkeysolutions.net/records/fda_inspections/biolife-plasma-services-lp/39cf2f99-d130-4068-9de1-e5821cf987e2) — classification: No Action Indicated (NAI), source: FDA, date: August 13, 2014
- [FDA Inspection 886632 - BioLife Plasma Services L.P. - 2014-07-08](https://www.globalkeysolutions.net/records/fda_inspections/biolife-plasma-services-lp/34565ffc-0e38-4f69-b106-0f18d2afda65) — classification: No Action Indicated (NAI), source: FDA, date: July 8, 2014
- [FDA Inspection 754383 - BioLife Plasma Services L.P. - 2011-11-22](https://www.globalkeysolutions.net/records/fda_inspections/biolife-plasma-services-lp/cde84fcb-8a79-4d68-bdd2-5d84b1598e43) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 22, 2011

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