Americord Registry LLC
FDA inspection history in Somerset, New Jersey, 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, at Somerset, New Jersey.
Cited most
Across all Americord Registry observations on file
- 21 CFR 1271.60What quarantine and other requirements apply before the donor-eligibility determination is complete?3
- 21 CFR 1271.270Records2
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 1271.160Establishment and maintenance of a quality program1
- 21 CFR 1271.180Procedures1
The complete Americord Registry file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Somerset, New Jersey
One Form 483 · 2025 · 17 observations
Latest: Form 483, Nov 17, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-11-17 | 483 Form 483 | Somerset, New Jersey | 17 | $99 |
Investigators on these documents
FEI number 3006988080 · most recent document Nov 17, 2025
About Americord Registry LLC
How many FDA Form 483s has Americord Registry LLC received?
FDA Intel has 1 Form 483 on file for Americord Registry LLC; the most recent is dated Nov 17, 2025.
When was Americord Registry LLC last inspected by FDA?
The most recent FDA inspection document on file for Americord Registry LLC is a Form 483 dated Nov 17, 2025, for the site in Somerset, New Jersey.
What did FDA cite at Americord Registry LLC?
The regulations cited most in the observations on file for Americord Registry LLC are 21 CFR 1271.60 (What quarantine and other requirements apply before the donor-eligibility determination is complete?), 3 times; 21 CFR 1271.270 (Records), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 2 times.