Medivis, Inc
FDA inspection history in New York, New York, 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 New York, New York.
Cited most
Across all Medivis observations on file
- ISO 13485:2016 Clause 7.3.7Definitions1
- 21 CFR 820.181Device master record1
The complete Medivis file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
New York, New York
One Form 483 · 2026 · 2 observations
Latest: Form 483, Mar 3, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-03-03 | 483 Form 483 | New York, New York | 2 | $99 |
Investigators on these documents
FEI number 3015536273 · most recent document Mar 3, 2026
About Medivis, Inc
How many FDA Form 483s has Medivis, Inc received?
FDA Intel has 1 Form 483 on file for Medivis, Inc; the most recent is dated Mar 3, 2026.
When was Medivis, Inc last inspected by FDA?
The most recent FDA inspection document on file for Medivis, Inc is a Form 483 dated Mar 3, 2026, for the site in New York, New York.
What did FDA cite at Medivis, Inc?
The regulations cited most in the observations on file for Medivis, Inc are ISO 13485:2016 Clause 7.3.7 (Definitions), 1 time; 21 CFR 820.181 (Device master record), 1 time.