LED Technologies
FDA inspection history in Greenwood Village, Colorado, 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 Greenwood Village, Colorado.
Cited most
Across all LED Technologies observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.22Quality audit1
- 21 CFR 820.40Document controls1
- 21 CFR 820.50(b)Purchasing controls1
The complete LED Technologies file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Greenwood Village, Colorado
One Form 483 · 2016 · 4 observations
Latest: Form 483, Jun 30, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-06-30 | 483 Form 483 | Greenwood Village, Colorado | 4 | $99 |
Investigators on these documents
FEI number 3006315288 · most recent document Jun 30, 2016
About LED Technologies
How many FDA Form 483s has LED Technologies received?
FDA Intel has 1 Form 483 on file for LED Technologies; the most recent is dated Jun 30, 2016.
When was LED Technologies last inspected by FDA?
The most recent FDA inspection document on file for LED Technologies is a Form 483 dated Jun 30, 2016, for the site in Greenwood Village, Colorado.
What did FDA cite at LED Technologies?
The regulations cited most in the observations on file for LED Technologies are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.22 (Quality audit), 1 time; 21 CFR 820.40 (Document controls), 1 time.