Alexza Pharmaceuticals, Inc
FDA inspection history in Mountain View, California, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Mountain View, California.
Cited most
Across all Alexza Pharmaceuticals observations on file
- 21 CFR 111
- 21 CFR 211.192Production record review1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete Alexza Pharmaceuticals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Mountain View, California
One Form 483 · 2015 · 2 observations
Latest: Form 483, May 21, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-05-21 | 483 Form 483 | Mountain View, California | 2 | $99 |
Investigators on these documents
FEI number 3007119522 · most recent document May 21, 2015
About Alexza Pharmaceuticals, Inc
How many FDA Form 483s has Alexza Pharmaceuticals, Inc received?
FDA Intel has 1 Form 483 on file for Alexza Pharmaceuticals, Inc; the most recent is dated May 21, 2015.
When was Alexza Pharmaceuticals, Inc last inspected by FDA?
The most recent FDA inspection document on file for Alexza Pharmaceuticals, Inc is a Form 483 dated May 21, 2015, for the site in Mountain View, California.
What did FDA cite at Alexza Pharmaceuticals, Inc?
The regulations cited most in the observations on file for Alexza Pharmaceuticals, Inc are 21 CFR 11, 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.68(b) (Automatic, mechanical, and electronic equipment), 1 time.