BioLife Plasma Services L.P.
FDA inspection history on file, 2026
- 1
- Form 483
Every document, by year
- Form 483
2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2026One Form 483.
Cited most
Across all BioLife Plasma Services observations on file
- 21 CFR 606.100Standard operating procedures1
- 21 CFR 630.10General donor eligibility requirements1
- 21 CFR 630.30Donation suitability requirements1
- 21 CFR 630.40Requirements for notifying deferred donors1
- 21 CFR 630.5Medical supervision1
The complete BioLife Plasma Services file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-03-20 | 483 Form 483 | — | 5 | $99 |
Investigators on these documents
FEI number 3023831018 · most recent document Mar 20, 2026
About BioLife Plasma Services L.P.
How many FDA Form 483s has BioLife Plasma Services L.P. received?
FDA Intel has 1 Form 483 on file for BioLife Plasma Services L.P.; the most recent is dated Mar 20, 2026.
When was BioLife Plasma Services L.P. last inspected by FDA?
The most recent FDA inspection document on file for BioLife Plasma Services L.P. is a Form 483 dated Mar 20, 2026.
What did FDA cite at BioLife Plasma Services L.P.?
The regulations cited most in the observations on file for BioLife Plasma Services L.P. are 21 CFR 606.100 (Standard operating procedures), 1 time; 21 CFR 630.10 (General donor eligibility requirements), 1 time; 21 CFR 630.30 (Donation suitability requirements), 1 time.