Baxalta Manufacturing Sàrl
FDA inspection history in NEUCHÂTEL, Switzerland, 2013
- 1
- Form 483
Every document, by year
- Form 483
2013: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2013One Form 483, at NEUCHÂTEL, Switzerland.
Cited most
Across all Baxalta Manufacturing Sàrl observations on file
- 21 CFR 211.192Production record review4
- 21 CFR 211.165Testing and release for distribution1
- 21 CFR 211.166Stability testing1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Baxalta Manufacturing Sàrl file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
NEUCHÂTEL, Switzerland
One Form 483 · 2013 · 6 observations
Latest: Form 483, Jul 12, 2013 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2013-07-12 | 483 Form 483 | NEUCHÂTEL, Switzerland | 6 | $99 |
Investigators on these documents
FEI number 3002689389 · most recent document Jul 12, 2013
About Baxalta Manufacturing Sàrl
How many FDA Form 483s has Baxalta Manufacturing Sàrl received?
FDA Intel has 1 Form 483 on file for Baxalta Manufacturing Sàrl; the most recent is dated Jul 12, 2013.
When was Baxalta Manufacturing Sàrl last inspected by FDA?
The most recent FDA inspection document on file for Baxalta Manufacturing Sàrl is a Form 483 dated Jul 12, 2013, for the site in NEUCHÂTEL, Switzerland.
What did FDA cite at Baxalta Manufacturing Sàrl?
The regulations cited most in the observations on file for Baxalta Manufacturing Sàrl are 21 CFR 211.192 (Production record review), 4 times; 21 CFR 211.165 (Testing and release for distribution), 1 time; 21 CFR 211.166 (Stability testing), 1 time.