Aarkish Pharmaceuticals NJ Inc
FDA inspection history in Fairfield, New Jersey, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Fairfield, New Jersey.
Cited most
Across all Aarkish Pharmaceuticals NJ observations on file
- 21 CFR 211.68Automatic, mechanical, and electronic equipment3
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.142Warehousing procedures1
- 21 CFR 211.188Batch production and control records1
The complete Aarkish Pharmaceuticals NJ file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Fairfield, New Jersey
One Form 483 · 2022 · 9 observations
Latest: Form 483, Aug 18, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-08-18 | 483 Form 483 | Fairfield, New Jersey | 9 | $99 |
Investigators on these documents
FEI number 3017532195 · most recent document Aug 18, 2022
About Aarkish Pharmaceuticals NJ Inc
How many FDA Form 483s has Aarkish Pharmaceuticals NJ Inc received?
FDA Intel has 1 Form 483 on file for Aarkish Pharmaceuticals NJ Inc; the most recent is dated Aug 18, 2022.
When was Aarkish Pharmaceuticals NJ Inc last inspected by FDA?
The most recent FDA inspection document on file for Aarkish Pharmaceuticals NJ Inc is a Form 483 dated Aug 18, 2022, for the site in Fairfield, New Jersey.
What did FDA cite at Aarkish Pharmaceuticals NJ Inc?
The regulations cited most in the observations on file for Aarkish Pharmaceuticals NJ Inc are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 3 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time.