Mannkind Corporation
FDA inspection history across 2 sites, 2018 to 2021
- 2
- Close-outs
- 1
- Form 483
Every document, by year
- Form 483
- Close-out
2018: one close-out letter; 2019: one close-out letter; 2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018–21Two close-out letters and one Form 483, at Danbury, Connecticut and Westlake Village, California.
Cited most
Across all Mannkind observations on file
- 21 CFR 211.68Automatic, mechanical, and electronic equipment1
The complete Mannkind file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Danbury, Connecticut
One Form 483 and one close-out letter · 2018 to 2021 · 1 observation
Latest: Form 483, Aug 6, 2021 →Westlake Village, California
One close-out letter · 2019
Latest: Close-out, Oct 23, 2019 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-08-06 | 483 Form 483 | Danbury, Connecticut | 1 | $99 |
| 2019-10-23 | Close-out Close-out letter | Westlake Village, California | — | $99 |
| 2018-10-05 | Close-out Close-out letter | Danbury, Connecticut | — | $99 |
FEI number 3005340341 · most recent document Aug 6, 2021
About Mannkind Corporation
How many FDA Form 483s has Mannkind Corporation received?
FDA Intel has 1 Form 483 on file for Mannkind Corporation; the most recent is dated Aug 6, 2021.
When was Mannkind Corporation last inspected by FDA?
The most recent FDA inspection document on file for Mannkind Corporation is a Form 483 dated Aug 6, 2021, for the site in Danbury, Connecticut.
What did FDA cite at Mannkind Corporation?
The regulations cited most in the observations on file for Mannkind Corporation are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 1 time.