FVS Holdings, Inc. (dba Green Valley Drugs)
FDA inspection history in Henderson, Nevada, 2013
- 1
- Form 483
Every document, by year
- Form 483
2013: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2013One Form 483, at Henderson, Nevada.
Cited most
Across all FVS Holdings, Inc. (dba Green Valley Drugs) observations on file
- 21 CFR 211.42(c)Design and construction features3
- 21 CFR 211.113(b)Control of microbiological contamination2
- 21 CFR 211.165(a)Testing and release for distribution2
- 21 CFR 211.130Packaging and labeling operations1
- 21 CFR 211.166(a)Stability testing1
The complete FVS Holdings, Inc. (dba Green Valley Drugs) file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Henderson, Nevada
One Form 483 · 2013 · 13 observations
Latest: Form 483, Mar 15, 2013 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2013-03-15 | 483 Form 483 | Henderson, Nevada | 13 | $99 |
Investigators on these documents
FEI number 3006306504 · most recent document Mar 15, 2013
About FVS Holdings, Inc. (dba Green Valley Drugs)
How many FDA Form 483s has FVS Holdings, Inc. (dba Green Valley Drugs) received?
FDA Intel has 1 Form 483 on file for FVS Holdings, Inc. (dba Green Valley Drugs); the most recent is dated Mar 15, 2013.
When was FVS Holdings, Inc. (dba Green Valley Drugs) last inspected by FDA?
The most recent FDA inspection document on file for FVS Holdings, Inc. (dba Green Valley Drugs) is a Form 483 dated Mar 15, 2013, for the site in Henderson, Nevada.
What did FDA cite at FVS Holdings, Inc. (dba Green Valley Drugs)?
The regulations cited most in the observations on file for FVS Holdings, Inc. (dba Green Valley Drugs) are 21 CFR 211.42(c) (Design and construction features), 3 times; 21 CFR 211.113(b) (Control of microbiological contamination), 2 times; 21 CFR 211.165(a) (Testing and release for distribution), 2 times.