Dee Cee Laboratories, Inc
FDA inspection history in White House, Tennessee, 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 White House, Tennessee.
Cited most
Across all Dee Cee Laboratories observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products2
- 21 CFR 211.166(c)(1)Stability testing1
- 21 CFR 211.180(e)(2)General requirements1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.67(b)Equipment cleaning and maintenance1
The complete Dee Cee Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
White House, Tennessee
One Form 483 · 2025 · 7 observations
Latest: Form 483, Aug 11, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-08-11 | 483 Form 483 | White House, Tennessee | 7 | $99 |
Investigators on these documents
FEI number 1023013 · most recent document Aug 11, 2025
About Dee Cee Laboratories, Inc
How many FDA Form 483s has Dee Cee Laboratories, Inc received?
FDA Intel has 1 Form 483 on file for Dee Cee Laboratories, Inc; the most recent is dated Aug 11, 2025.
When was Dee Cee Laboratories, Inc last inspected by FDA?
The most recent FDA inspection document on file for Dee Cee Laboratories, Inc is a Form 483 dated Aug 11, 2025, for the site in White House, Tennessee.
What did FDA cite at Dee Cee Laboratories, Inc?
The regulations cited most in the observations on file for Dee Cee Laboratories, Inc are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 2 times; 21 CFR 211.166(c)(1) (Stability testing), 1 time; 21 CFR 211.180(e)(2) (General requirements), 1 time.