Keystone Manufacturing LLC
FDA inspection history in Kalamazoo, Michigan, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Kalamazoo, Michigan.
Cited most
Across all Keystone Manufacturing observations on file
- 21 CFR 820.22Quality audit2
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.50Purchasing controls1
- 21 CFR 820.90(a)Nonconforming product1
The complete Keystone Manufacturing file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Kalamazoo, Michigan
One Form 483 · 2019 · 5 observations
Latest: Form 483, Dec 11, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-12-11 | 483 Form 483 | Kalamazoo, Michigan | 5 | $99 |
Investigators on these documents
FEI number 3008236846 · most recent document Dec 11, 2019
About Keystone Manufacturing LLC
How many FDA Form 483s has Keystone Manufacturing LLC received?
FDA Intel has 1 Form 483 on file for Keystone Manufacturing LLC; the most recent is dated Dec 11, 2019.
When was Keystone Manufacturing LLC last inspected by FDA?
The most recent FDA inspection document on file for Keystone Manufacturing LLC is a Form 483 dated Dec 11, 2019, for the site in Kalamazoo, Michigan.
What did FDA cite at Keystone Manufacturing LLC?
The regulations cited most in the observations on file for Keystone Manufacturing LLC are 21 CFR 820.22 (Quality audit), 2 times; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.50 (Purchasing controls), 1 time.