June Jacobs Labs, LLC
FDA inspection history in Moonachie, 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 Moonachie, New Jersey.
Cited most
Across all June Jacobs Labs observations on file
- 21 CFR 211.122(a)Materials examination and usage criteria1
- 21 CFR 211.165(a)Testing and release for distribution1
- 21 CFR 211.192Production record review1
The complete June Jacobs Labs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Moonachie, New Jersey
One Form 483 · 2024 · 3 observations
Latest: Form 483, Nov 4, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-11-04 | 483 Form 483 | Moonachie, New Jersey | 3 | $99 |
Investigators on these documents
FEI number 3002832995 · most recent document Nov 4, 2024
About June Jacobs Labs, LLC
How many FDA Form 483s has June Jacobs Labs, LLC received?
FDA Intel has 1 Form 483 on file for June Jacobs Labs, LLC; the most recent is dated Nov 4, 2024.
When was June Jacobs Labs, LLC last inspected by FDA?
The most recent FDA inspection document on file for June Jacobs Labs, LLC is a Form 483 dated Nov 4, 2024, for the site in Moonachie, New Jersey.
What did FDA cite at June Jacobs Labs, LLC?
The regulations cited most in the observations on file for June Jacobs Labs, LLC are 21 CFR 211.122(a) (Materials examination and usage criteria), 1 time; 21 CFR 211.165(a) (Testing and release for distribution), 1 time; 21 CFR 211.192 (Production record review), 1 time.