Diversified Chemical Products
FDA inspection history in Wilmington, Delaware, 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 Wilmington, Delaware.
Cited most
Across all Diversified Chemical Products observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Diversified Chemical Products file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Wilmington, Delaware
One Form 483 · 2025 · 2 observations
Latest: Form 483, Jan 31, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-01-31 | 483 Form 483 | Wilmington, Delaware | 2 | $99 |
Investigators on these documents
Christian F. Gomez Lugo (1)Marian E. Ramirez (1)Yoriann M. Cabrera Bartolomei (1)
FEI number 1000071265 · most recent document Jan 31, 2025
About Diversified Chemical Products
How many FDA Form 483s has Diversified Chemical Products received?
FDA Intel has 1 Form 483 on file for Diversified Chemical Products; the most recent is dated Jan 31, 2025.
When was Diversified Chemical Products last inspected by FDA?
The most recent FDA inspection document on file for Diversified Chemical Products is a Form 483 dated Jan 31, 2025, for the site in Wilmington, Delaware.
What did FDA cite at Diversified Chemical Products?
The regulations cited most in the observations on file for Diversified Chemical Products are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.