BAXALTA US INC.
FDA inspection history in LOS ANGELES, California, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at LOS ANGELES, California.
Cited most
Across all BAXALTA US observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.160General requirements1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.42Design and construction features1
- 21 CFR 211.56Sanitation1
The complete BAXALTA US file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
LOS ANGELES, California
One Form 483 · 2023
Latest: Form 483, May 31, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-05-31 | 483 Form 483 | LOS ANGELES, California | — | $99 |
Investigators on these documents
FEI number 2011021 · most recent document May 31, 2023
About BAXALTA US INC.
How many FDA Form 483s has BAXALTA US INC. received?
FDA Intel has 1 Form 483 on file for BAXALTA US INC.; the most recent is dated May 31, 2023.
When was BAXALTA US INC. last inspected by FDA?
The most recent FDA inspection document on file for BAXALTA US INC. is a Form 483 dated May 31, 2023, for the site in LOS ANGELES, California.
What did FDA cite at BAXALTA US INC.?
The regulations cited most in the observations on file for BAXALTA US INC. are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.