Professional Partners Inc./ Westcliff Compounding Pharmacy
FDA inspection history in Newport Beach, California, 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 Newport Beach, California.
Cited most
Across all Professional Partners Inc./ Westcliff Compounding Pharmacy observations on file
- 21 CFR 211.113(b)Control of microbiological contamination1
- 21 CFR 211.160(b)(4)General requirements1
- 21 CFR 211.165(b)Testing and release for distribution1
- 21 CFR 211.166(a)Stability testing1
- 21 CFR 211.192Production record review1
The complete Professional Partners Inc./ Westcliff Compounding Pharmacy file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Newport Beach, California
One Form 483 · 2016 · 8 observations
Latest: Form 483, May 9, 2016 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2016-05-09 | 483 Form 483 | Newport Beach, California | 8 | $99 |
Investigators on these documents
FEI number 3012266548 · most recent document May 9, 2016
About Professional Partners Inc./ Westcliff Compounding Pharmacy
How many FDA Form 483s has Professional Partners Inc./ Westcliff Compounding Pharmacy received?
FDA Intel has 1 Form 483 on file for Professional Partners Inc./ Westcliff Compounding Pharmacy; the most recent is dated May 9, 2016.
When was Professional Partners Inc./ Westcliff Compounding Pharmacy last inspected by FDA?
The most recent FDA inspection document on file for Professional Partners Inc./ Westcliff Compounding Pharmacy is a Form 483 dated May 9, 2016, for the site in Newport Beach, California.
What did FDA cite at Professional Partners Inc./ Westcliff Compounding Pharmacy?
The regulations cited most in the observations on file for Professional Partners Inc./ Westcliff Compounding Pharmacy are 21 CFR 211.113(b) (Control of microbiological contamination), 1 time; 21 CFR 211.160(b)(4) (General requirements), 1 time; 21 CFR 211.165(b) (Testing and release for distribution), 1 time.