Continental Manufacturing Chemist
FDA inspection history in Huxley, Iowa, 2019 to 2023
- 2
- Form 483s
Every document, by year
- Form 483
2019: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Huxley, Iowa.
- 2019The longest 483 on file: 5 observations over 7 pages at Huxley, Iowa.
- 2023One Form 483, at Huxley, Iowa.
Cited most
Across all Continental Manufacturing Chemist observations on file
- 21 CFR 211.68(a)Automatic, mechanical, and electronic equipment4
- 21 CFR 211.67(b)Equipment cleaning and maintenance2
- 21 CFR 211.84(b)Testing and approval or rejection of components, drug product containers, and closures2
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Continental Manufacturing Chemist 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
Huxley, Iowa
Two Form 483s · 2019 to 2023 · 9 observations
Latest: Form 483, May 10, 2023 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-05-10 | 483 Form 483 | Huxley, Iowa | 4 | $99 |
| 2019-07-30 | 483 Form 483 | Huxley, Iowa | 5 | $99 |
Investigators on these documents
FEI number 3014469173 · most recent document May 10, 2023
About Continental Manufacturing Chemist
How many FDA Form 483s has Continental Manufacturing Chemist received?
FDA Intel has 2 Form 483s on file for Continental Manufacturing Chemist; the most recent is dated May 10, 2023.
When was Continental Manufacturing Chemist last inspected by FDA?
The most recent FDA inspection document on file for Continental Manufacturing Chemist is a Form 483 dated May 10, 2023, for the site in Huxley, Iowa.
What did FDA cite at Continental Manufacturing Chemist?
The regulations cited most in the observations on file for Continental Manufacturing Chemist are 21 CFR 211.68(a) (Automatic, mechanical, and electronic equipment), 4 times; 21 CFR 211.67(b) (Equipment cleaning and maintenance), 2 times; 21 CFR 211.84(b) (Testing and approval or rejection of components, drug product containers, and closures), 2 times.