Triangle Manufacturing Co. Inc
FDA inspection history in Upper Saddle River, 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 Upper Saddle River, New Jersey.
Cited most
Across all Triangle Manufacturing Co. observations on file
- 21 CFR 820.25(b)Personnel1
- 21 CFR 820.75(a)Process validation1
The complete Triangle Manufacturing Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Upper Saddle River, New Jersey
One Form 483 · 2025 · 2 observations
Latest: Form 483, Jun 12, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-06-12 | 483 Form 483 | Upper Saddle River, New Jersey | 2 | $99 |
Investigators on these documents
FEI number 1000491390 · most recent document Jun 12, 2025
About Triangle Manufacturing Co. Inc
How many FDA Form 483s has Triangle Manufacturing Co. Inc received?
FDA Intel has 1 Form 483 on file for Triangle Manufacturing Co. Inc; the most recent is dated Jun 12, 2025.
When was Triangle Manufacturing Co. Inc last inspected by FDA?
The most recent FDA inspection document on file for Triangle Manufacturing Co. Inc is a Form 483 dated Jun 12, 2025, for the site in Upper Saddle River, New Jersey.
What did FDA cite at Triangle Manufacturing Co. Inc?
The regulations cited most in the observations on file for Triangle Manufacturing Co. Inc are 21 CFR 820.25(b) (Personnel), 1 time; 21 CFR 820.75(a) (Process validation), 1 time.