Precision Pharmacy Center LLC
FDA inspection history in Brea, California, 2015 to 2016
- 2
- Form 483s
- 1
- Warning letter
Every document, by year
- Warning letter
- Form 483
2015: one Form 483; 2016: one warning letter and one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015–16Two Form 483s and one warning letter, at Brea, California.
- 2015The longest 483 on file: 6 observations over 3 pages at Brea, California.
Cited most
Across all Precision Pharmacy Center observations on file
- 21 CFR 211.165(a)Testing and release for distribution2
- 21 CFR 211.166(a)Stability testing2
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.167(a)Special testing requirements1
The complete Precision Pharmacy Center file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Brea, California
Two Form 483s and one warning letter · 2015 to 2016 · 9 observations
Latest: Warning letter, Nov 15, 2016 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-11-15 | Warning letter Warning letter | Brea, California | — | $99 |
| 2016-06-17 | 483 Form 483 | Brea, California | 3 | $99 |
| 2015-04-01 | 483 Form 483 | Brea, California | 6 | $99 |
Investigators on these documents
FEI number 3011432609 · most recent document Nov 15, 2016
About Precision Pharmacy Center LLC
How many FDA Form 483s has Precision Pharmacy Center LLC received?
FDA Intel has 2 Form 483s on file for Precision Pharmacy Center LLC; the most recent is dated Jun 17, 2016.
When was Precision Pharmacy Center LLC last inspected by FDA?
The most recent FDA inspection document on file for Precision Pharmacy Center LLC is a Form 483 dated Jun 17, 2016, for the site in Brea, California.
What did FDA cite at Precision Pharmacy Center LLC?
The regulations cited most in the observations on file for Precision Pharmacy Center LLC are 21 CFR 211.165(a) (Testing and release for distribution), 2 times; 21 CFR 211.166(a) (Stability testing), 2 times; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time.
Has Precision Pharmacy Center LLC received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Precision Pharmacy Center LLC; the most recent is dated Nov 15, 2016.