Adaptimmune LLC
FDA inspection history in Philadelphia, Pennsylvania, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Philadelphia, Pennsylvania.
Cited most
Across all Adaptimmune observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.180General requirements1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures1
The complete Adaptimmune file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Philadelphia, Pennsylvania
One Form 483 · 2024 · 5 observations
Latest: Form 483, Apr 5, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-04-05 | 483 Form 483 | Philadelphia, Pennsylvania | 5 | $99 |
Investigators on these documents
FEI number 3013525969 · most recent document Apr 5, 2024
About Adaptimmune LLC
How many FDA Form 483s has Adaptimmune LLC received?
FDA Intel has 1 Form 483 on file for Adaptimmune LLC; the most recent is dated Apr 5, 2024.
When was Adaptimmune LLC last inspected by FDA?
The most recent FDA inspection document on file for Adaptimmune LLC is a Form 483 dated Apr 5, 2024, for the site in Philadelphia, Pennsylvania.
What did FDA cite at Adaptimmune LLC?
The regulations cited most in the observations on file for Adaptimmune LLC are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.180 (General requirements), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.