Specialty Vision Lie
FDA inspection history in Ridgefield Park, 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 Ridgefield Park, New Jersey.
Cited most
Across all Specialty Vision Lie observations on file
- 21 CFR 820.20(e)Management responsibility1
- 21 CFR 820.80(e)Receiving, in-process, and finished device acceptance1
- 21 CFR 820.90(b)(2)Nonconforming product1
The complete Specialty Vision Lie file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Ridgefield Park, New Jersey
One Form 483 · 2024 · 3 observations
Latest: Form 483, Dec 19, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-12-19 | 483 Form 483 | Ridgefield Park, New Jersey | 3 | $99 |
Investigators on these documents
FEI number 3011271964 · most recent document Dec 19, 2024
About Specialty Vision Lie
How many FDA Form 483s has Specialty Vision Lie received?
FDA Intel has 1 Form 483 on file for Specialty Vision Lie; the most recent is dated Dec 19, 2024.
When was Specialty Vision Lie last inspected by FDA?
The most recent FDA inspection document on file for Specialty Vision Lie is a Form 483 dated Dec 19, 2024, for the site in Ridgefield Park, New Jersey.
What did FDA cite at Specialty Vision Lie?
The regulations cited most in the observations on file for Specialty Vision Lie are 21 CFR 820.20(e) (Management responsibility), 1 time; 21 CFR 820.80(e) (Receiving, in-process, and finished device acceptance), 1 time; 21 CFR 820.90(b)(2) (Nonconforming product), 1 time.