Custom RX LLC, dba Custom RX Compounding Pharmacy
FDA inspection history in Richfield, Minnesota, 2014
- 1
- Form 483
Every document, by year
- Form 483
2014: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2014One Form 483, at Richfield, Minnesota.
Cited most
Across all Custom RX LLC, dba Custom RX Compounding Pharmacy observations on file
- 21 CFR 211.110Sampling and testing of in-process materials and drug products3
- 21 CFR 211.113(a)Control of microbiological contamination1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.165(b)Testing and release for distribution1
- 21 CFR 211.166(b)Stability testing1
The complete Custom RX LLC, dba Custom RX Compounding Pharmacy file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Richfield, Minnesota
One Form 483 · 2014 · 9 observations
Latest: Form 483, Aug 28, 2014 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2014-08-28 | 483 Form 483 | Richfield, Minnesota | 9 | $99 |
Investigators on these documents
FEI number 3003316042 · most recent document Aug 28, 2014
About Custom RX LLC, dba Custom RX Compounding Pharmacy
How many FDA Form 483s has Custom RX LLC, dba Custom RX Compounding Pharmacy received?
FDA Intel has 1 Form 483 on file for Custom RX LLC, dba Custom RX Compounding Pharmacy; the most recent is dated Aug 28, 2014.
When was Custom RX LLC, dba Custom RX Compounding Pharmacy last inspected by FDA?
The most recent FDA inspection document on file for Custom RX LLC, dba Custom RX Compounding Pharmacy is a Form 483 dated Aug 28, 2014, for the site in Richfield, Minnesota.
What did FDA cite at Custom RX LLC, dba Custom RX Compounding Pharmacy?
The regulations cited most in the observations on file for Custom RX LLC, dba Custom RX Compounding Pharmacy are 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 3 times; 21 CFR 211.113(a) (Control of microbiological contamination), 1 time; 21 CFR 211.160(b) (General requirements), 1 time.