Venus Concept
FDA inspection history in San Jose, California, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at San Jose, California.
Cited most
Across all Venus Concept observations on file
- 21 CFR 820.100(b)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
The complete Venus Concept file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
San Jose, California
One Form 483 · 2020 · 2 observations
Latest: Form 483, Jan 16, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-01-16 | 483 Form 483 | San Jose, California | 2 | $99 |
Investigators on these documents
FEI number 3006515340 · most recent document Jan 16, 2020
About Venus Concept
How many FDA Form 483s has Venus Concept received?
FDA Intel has 1 Form 483 on file for Venus Concept; the most recent is dated Jan 16, 2020.
When was Venus Concept last inspected by FDA?
The most recent FDA inspection document on file for Venus Concept is a Form 483 dated Jan 16, 2020, for the site in San Jose, California.
What did FDA cite at Venus Concept?
The regulations cited most in the observations on file for Venus Concept are 21 CFR 820.100(b) (Corrective and preventive action), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.