FEI 3011121261
FDA inspection history in Cleveland, Ohio, 2026
- 1
- Form 483
Every document, by year
- Form 483
2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2026One Form 483, at Cleveland, Ohio.
Cited most
Across all site observations on file
- 21 CFR 212.30(a)What requirements must my facilities and equipment meet?2
- 21 CFR 212.50(e)What production and process controls must I have?1
- 21 CFR 361.1(d)(1)(iv)Radioactive drugs for certain research uses1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Cleveland, Ohio
One Form 483 · 2026 · 4 observations
Latest: Form 483, Feb 17, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-02-17 | 483 Form 483 | Cleveland, Ohio | 4 | $99 |
Investigators on these documents
FEI number 3011121261 · most recent document Feb 17, 2026
About FEI 3011121261
How many FDA Form 483s has FEI 3011121261 received?
FDA Intel has 1 Form 483 on file for FEI 3011121261; the most recent is dated Feb 17, 2026.
When was FEI 3011121261 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3011121261 is a Form 483 dated Feb 17, 2026, for the site in Cleveland, Ohio.
What did FDA cite at FEI 3011121261?
The regulations cited most in the observations on file for FEI 3011121261 are 21 CFR 212.30(a) (What requirements must my facilities and equipment meet?), 2 times; 21 CFR 212.50(e) (What production and process controls must I have?), 1 time; 21 CFR 361.1(d)(1)(iv) (Radioactive drugs for certain research uses), 1 time.