Keystone Industries
FDA inspection history in Cherry Hill, New Jersey, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Cherry Hill, New Jersey.
Cited most
Across all Keystone Industries observations on file
- 21 CFR 820.198(a)Complaint files2
- 21 CFR 8201
- 21 CFR 803.50(a)(1)If I am a manufacturer, what reporting requirements apply to me?1
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.22Quality audit1
The complete Keystone Industries file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Cherry Hill, New Jersey
One Form 483 · 2025 · 7 observations
Latest: Form 483, Jul 25, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-07-25 | 483 Form 483 | Cherry Hill, New Jersey | 7 | $99 |
Investigators on these documents
FEI number 1000121639 · most recent document Jul 25, 2025
About Keystone Industries
How many FDA Form 483s has Keystone Industries received?
FDA Intel has 1 Form 483 on file for Keystone Industries; the most recent is dated Jul 25, 2025.
When was Keystone Industries last inspected by FDA?
The most recent FDA inspection document on file for Keystone Industries is a Form 483 dated Jul 25, 2025, for the site in Cherry Hill, New Jersey.
What did FDA cite at Keystone Industries?
The regulations cited most in the observations on file for Keystone Industries are 21 CFR 820.198(a) (Complaint files), 2 times; 21 CFR 820, 1 time; 21 CFR 803.50(a)(1) (If I am a manufacturer, what reporting requirements apply to me?), 1 time.