Maxx Orthopedics Inc
FDA inspection history in Plymouth Meeting, Pennsylvania, 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 Plymouth Meeting, Pennsylvania.
Cited most
Across all Maxx Orthopedics observations on file
- 21 CFR 820.50Purchasing controls1
- 21 CFR 820.70Production and process controls1
The complete Maxx Orthopedics file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Plymouth Meeting, Pennsylvania
One Form 483 · 2015 · 2 observations
Latest: Form 483, Feb 27, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-02-27 | 483 Form 483 | Plymouth Meeting, Pennsylvania | 2 | $99 |
Investigators on these documents
FEI number 3009341131 · most recent document Feb 27, 2015
About Maxx Orthopedics Inc
How many FDA Form 483s has Maxx Orthopedics Inc received?
FDA Intel has 1 Form 483 on file for Maxx Orthopedics Inc; the most recent is dated Feb 27, 2015.
When was Maxx Orthopedics Inc last inspected by FDA?
The most recent FDA inspection document on file for Maxx Orthopedics Inc is a Form 483 dated Feb 27, 2015, for the site in Plymouth Meeting, Pennsylvania.
What did FDA cite at Maxx Orthopedics Inc?
The regulations cited most in the observations on file for Maxx Orthopedics Inc are 21 CFR 820.50 (Purchasing controls), 1 time; 21 CFR 820.70 (Production and process controls), 1 time.