Medshift
FDA inspection history in Charlotte, North Carolina, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Charlotte, North Carolina.
Cited most
Across all Medshift observations on file
- 21 CFR 820.50(a)(1)Purchasing controls3
- 21 CFR 820.181Device master record1
- 21 CFR 820.184Device history record1
- 21 CFR 820.20(b)(3)(ii)Management responsibility1
- 21 CFR 820.25(b)Personnel1
The complete Medshift file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Charlotte, North Carolina
One Form 483 · 2024 · 10 observations
Latest: Form 483, Dec 13, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-12-13 | 483 Form 483 | Charlotte, North Carolina | 10 | $99 |
Investigators on these documents
FEI number 3013462594 · most recent document Dec 13, 2024
About Medshift
How many FDA Form 483s has Medshift received?
FDA Intel has 1 Form 483 on file for Medshift; the most recent is dated Dec 13, 2024.
When was Medshift last inspected by FDA?
The most recent FDA inspection document on file for Medshift is a Form 483 dated Dec 13, 2024, for the site in Charlotte, North Carolina.
What did FDA cite at Medshift?
The regulations cited most in the observations on file for Medshift are 21 CFR 820.50(a)(1) (Purchasing controls), 3 times; 21 CFR 820.181 (Device master record), 1 time; 21 CFR 820.184 (Device history record), 1 time.