Protech Leaded Eyewear
FDA inspection history in Lake Park, Florida, 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 Lake Park, Florida.
Cited most
Across all Protech Leaded Eyewear observations on file
- 21 CFR 8201
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.30(a)Design controls1
The complete Protech Leaded Eyewear file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Lake Park, Florida
One Form 483 · 2025 · 3 observations
Latest: Form 483, Mar 10, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-03-10 | 483 Form 483 | Lake Park, Florida | 3 | $99 |
Investigators on these documents
FEI number 1000488948 · most recent document Mar 10, 2025
About Protech Leaded Eyewear
How many FDA Form 483s has Protech Leaded Eyewear received?
FDA Intel has 1 Form 483 on file for Protech Leaded Eyewear; the most recent is dated Mar 10, 2025.
When was Protech Leaded Eyewear last inspected by FDA?
The most recent FDA inspection document on file for Protech Leaded Eyewear is a Form 483 dated Mar 10, 2025, for the site in Lake Park, Florida.
What did FDA cite at Protech Leaded Eyewear?
The regulations cited most in the observations on file for Protech Leaded Eyewear are 21 CFR 820, 1 time; 21 CFR 820.198(a) (Complaint files), 1 time; 21 CFR 820.22 (Quality audit), 1 time.