ENGLEWOOD LAB, INC.
FDA inspection history in TOTOWA, New Jersey, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at TOTOWA, New Jersey.
Cited most
Across all ENGLEWOOD LAB observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.67(a)Equipment cleaning and maintenance1
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures1
The complete ENGLEWOOD LAB file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
TOTOWA, New Jersey
One Form 483 · 2025 · 4 observations
Latest: Form 483, Apr 23, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-04-23 | 483 Form 483 | TOTOWA, New Jersey | 4 | $99 |
Investigators on these documents
FEI number 3013020160 · most recent document Apr 23, 2025
About ENGLEWOOD LAB, INC.
How many FDA Form 483s has ENGLEWOOD LAB, INC. received?
FDA Intel has 1 Form 483 on file for ENGLEWOOD LAB, INC.; the most recent is dated Apr 23, 2025.
When was ENGLEWOOD LAB, INC. last inspected by FDA?
The most recent FDA inspection document on file for ENGLEWOOD LAB, INC. is a Form 483 dated Apr 23, 2025, for the site in TOTOWA, New Jersey.
What did FDA cite at ENGLEWOOD LAB, INC.?
The regulations cited most in the observations on file for ENGLEWOOD LAB, INC. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time; 21 CFR 211.67(a) (Equipment cleaning and maintenance), 1 time.