Mannkind Corporation
FDA inspection history in Marlborough, Massachusetts, 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 Marlborough, Massachusetts.
Cited most
Across all Mannkind observations on file
- 21 CFR 820.30(g)Design controls2
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.250(b)Statistical techniques1
The complete Mannkind file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Marlborough, Massachusetts
One Form 483 · 2024 · 5 observations
Latest: Form 483, Oct 3, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-10-03 | 483 Form 483 | Marlborough, Massachusetts | 5 | $99 |
Investigators on these documents
FEI number 3003154078 · most recent document Oct 3, 2024
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 Oct 3, 2024.
When was Mannkind Corporation last inspected by FDA?
The most recent FDA inspection document on file for Mannkind Corporation is a Form 483 dated Oct 3, 2024, for the site in Marlborough, Massachusetts.
What did FDA cite at Mannkind Corporation?
The regulations cited most in the observations on file for Mannkind Corporation are 21 CFR 820.30(g) (Design controls), 2 times; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.