Welch, Holme & Clark Co., Inc
FDA inspection history in Newark, New Jersey, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Newark, New Jersey.
Cited most
Across all Welch, Holme & Clark Co. observations on file
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.25(a)Personnel qualifications1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete Welch, Holme & Clark Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Newark, New Jersey
One Form 483 · 2024 · 3 observations
Latest: Form 483, Jul 10, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-07-10 | 483 Form 483 | Newark, New Jersey | 3 | $99 |
Investigators on these documents
FEI number 2211876 · most recent document Jul 10, 2024
About Welch, Holme & Clark Co., Inc
How many FDA Form 483s has Welch, Holme & Clark Co., Inc received?
FDA Intel has 1 Form 483 on file for Welch, Holme & Clark Co., Inc; the most recent is dated Jul 10, 2024.
When was Welch, Holme & Clark Co., Inc last inspected by FDA?
The most recent FDA inspection document on file for Welch, Holme & Clark Co., Inc is a Form 483 dated Jul 10, 2024, for the site in Newark, New Jersey.
What did FDA cite at Welch, Holme & Clark Co., Inc?
The regulations cited most in the observations on file for Welch, Holme & Clark Co., Inc are 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time; 21 CFR 211.25(a) (Personnel qualifications), 1 time; 21 CFR 211.68(b) (Automatic, mechanical, and electronic equipment), 1 time.