Wexler Surgical, Inc
FDA inspection history in Houston, Texas, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Houston, Texas.
Cited most
Across all Wexler Surgical observations on file
- 21 CFR 820.30(g)Design controls2
- 21 CFR 820.120(d)Device labeling1
- 21 CFR 820.181Device master record1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.80(e)Receiving, in-process, and finished device acceptance1
The complete Wexler Surgical file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Houston, Texas
One Form 483 · 2015 · 6 observations
Latest: Form 483, Mar 20, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-03-20 | 483 Form 483 | Houston, Texas | 6 | $99 |
Investigators on these documents
FEI number 1000160162 · most recent document Mar 20, 2015
About Wexler Surgical, Inc
How many FDA Form 483s has Wexler Surgical, Inc received?
FDA Intel has 1 Form 483 on file for Wexler Surgical, Inc; the most recent is dated Mar 20, 2015.
When was Wexler Surgical, Inc last inspected by FDA?
The most recent FDA inspection document on file for Wexler Surgical, Inc is a Form 483 dated Mar 20, 2015, for the site in Houston, Texas.
What did FDA cite at Wexler Surgical, Inc?
The regulations cited most in the observations on file for Wexler Surgical, Inc are 21 CFR 820.30(g) (Design controls), 2 times; 21 CFR 820.120(d) (Device labeling), 1 time; 21 CFR 820.181 (Device master record), 1 time.