FEI 3006358789
FDA inspection history in Burlington, 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 Burlington, Kentucky.
Cited most
Across all site observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.122(a)Materials examination and usage criteria1
- 21 CFR 211.130Packaging and labeling operations1
- 21 CFR 211.25(a)Personnel qualifications1
The complete site file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Burlington, Kentucky
One Form 483 · 2016 · 4 observations
Latest: Form 483, Jul 7, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-07-07 | 483 Form 483 | Burlington, Kentucky | 4 | $99 |
Investigators on these documents
FEI number 3006358789 · most recent document Jul 7, 2016
About FEI 3006358789
How many FDA Form 483s has FEI 3006358789 received?
FDA Intel has 1 Form 483 on file for FEI 3006358789; the most recent is dated Jul 7, 2016.
When was FEI 3006358789 last inspected by FDA?
The most recent FDA inspection document on file for FEI 3006358789 is a Form 483 dated Jul 7, 2016, for the site in Burlington, Kentucky.
What did FDA cite at FEI 3006358789?
The regulations cited most in the observations on file for FEI 3006358789 are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.122(a) (Materials examination and usage criteria), 1 time; 21 CFR 211.130 (Packaging and labeling operations), 1 time.