# FDA Inspection 1019232 - BioLife Plasma Services LP - July 19, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/biolife-plasma-services-lp/6dfaad69-ffa9-47d9-bcce-cb483a4a9792
Source feed: FDA_Inspections

> FDA Inspection 1019232 for BioLife Plasma Services LP on July 19, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019232
- Company Name: BioLife Plasma Services LP
- Inspection Date: 2017-07-19
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

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- [FDA Inspection 933766 - 2015-07-09](https://www.globalkeysolutions.net/records/fda_inspections/biolife-plasma-services-lp/9e865b30-14a7-4f14-b3bb-b4a5c9adaf5f)

Company: https://www.globalkeysolutions.net/companies/biolife-plasma-services-lp/b1074162-76f8-4c27-9457-609737894a76

Office: https://www.globalkeysolutions.net/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d
