Quality Chemical Laboratories
FDA inspection history in Wilmington, North Carolina, 2017 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2017: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Wilmington, North Carolina.
- 2017The longest 483 on file: 2 observations over 6 pages at Wilmington, North Carolina.
- 2024One Form 483, at Wilmington, North Carolina.
Cited most
Across all Quality Chemical Laboratories observations on file
- 21 CFR 211.100(b)Written procedures; deviations1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.63Equipment design, size, and location1
The complete Quality Chemical Laboratories file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Wilmington, North Carolina
Two Form 483s · 2017 to 2024 · 4 observations
Latest: Form 483, Nov 20, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-20 | 483 Form 483 | Wilmington, North Carolina | 2 | $99 |
| 2017-07-27 | 483 Form 483 | Wilmington, North Carolina | 2 | $99 |
Investigators on these documents
FEI number 3002323490 · most recent document Nov 20, 2024
About Quality Chemical Laboratories
How many FDA Form 483s has Quality Chemical Laboratories received?
FDA Intel has 2 Form 483s on file for Quality Chemical Laboratories; the most recent is dated Nov 20, 2024.
When was Quality Chemical Laboratories last inspected by FDA?
The most recent FDA inspection document on file for Quality Chemical Laboratories is a Form 483 dated Nov 20, 2024, for the site in Wilmington, North Carolina.
What did FDA cite at Quality Chemical Laboratories?
The regulations cited most in the observations on file for Quality Chemical Laboratories are 21 CFR 211.100(b) (Written procedures; deviations), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.