BioLife Plasma Services L.P.
FDA inspection history in Kokomo, Indiana, 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, at Kokomo, Indiana.
Cited most
Across all BioLife Plasma Services observations on file
- 21 CFR 601.12Changes to an approved application1
- 21 CFR 606.160Records1
- 21 CFR 606.171Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services1
The complete BioLife Plasma Services file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Kokomo, Indiana
One Form 483 · 2026 · 3 observations
Latest: Form 483, Feb 20, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-02-20 | 483 Form 483 | Kokomo, Indiana | 3 | $99 |
Investigators on these documents
FEI number 3004582762 · most recent document Feb 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 Feb 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 Feb 20, 2026, for the site in Kokomo, Indiana.
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 601.12 (Changes to an approved application), 1 time; 21 CFR 606.160 (Records), 1 time; 21 CFR 606.171 (Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services), 1 time.