Cardinal Spine
FDA inspection history in Louisville, Kentucky, 2016
- 1
- Form 483
Every document, by year
- Form 483
2016: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016One Form 483, at Louisville, Kentucky.
Cited most
Across all Cardinal Spine observations on file
- 21 CFR 820.184Device history record1
- 21 CFR 820.80Receiving, in-process, and finished device acceptance1
The complete Cardinal Spine file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Louisville, Kentucky
One Form 483 · 2016 · 2 observations
Latest: Form 483, Nov 16, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-11-16 | 483 Form 483 | Louisville, Kentucky | 2 | $99 |
Investigators on these documents
FEI number 3010039129 · most recent document Nov 16, 2016
About Cardinal Spine
How many FDA Form 483s has Cardinal Spine received?
FDA Intel has 1 Form 483 on file for Cardinal Spine; the most recent is dated Nov 16, 2016.
When was Cardinal Spine last inspected by FDA?
The most recent FDA inspection document on file for Cardinal Spine is a Form 483 dated Nov 16, 2016, for the site in Louisville, Kentucky.
What did FDA cite at Cardinal Spine?
The regulations cited most in the observations on file for Cardinal Spine are 21 CFR 820.184 (Device history record), 1 time; 21 CFR 820.80 (Receiving, in-process, and finished device acceptance), 1 time.