Cryobank America LLC
FDA inspection history on file, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483.
Cited most
Across all Cryobank America observations on file
- 21 CFR 1271.47What procedures must I establish and maintain?1
- 21 CFR 1271.55What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?1
The complete Cryobank America 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 |
|---|---|---|---|---|
| 2025-01-13 | 483 Form 483 | — | 2 | $99 |
Investigators on these documents
FEI number 3013912801 · most recent document Jan 13, 2025
About Cryobank America LLC
How many FDA Form 483s has Cryobank America LLC received?
FDA Intel has 1 Form 483 on file for Cryobank America LLC; the most recent is dated Jan 13, 2025.
When was Cryobank America LLC last inspected by FDA?
The most recent FDA inspection document on file for Cryobank America LLC is a Form 483 dated Jan 13, 2025.
What did FDA cite at Cryobank America LLC?
The regulations cited most in the observations on file for Cryobank America LLC are 21 CFR 1271.47 (What procedures must I establish and maintain?), 1 time; 21 CFR 1271.55 (What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?), 1 time.