Leiter's Cambrian Park Drugs, Inc.
FDA inspection history in San Jose, California, 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 San Jose, California.
Cited most
Across all Leiter's Cambrian Park Drugs observations on file
- 21 CFR 211.42Design and construction features4
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.192Production record review2
- 21 CFR 211.160General requirements1
- 21 CFR 211.167Special testing requirements1
The complete Leiter's Cambrian Park Drugs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
San Jose, California
One Form 483 · 2013 · 15 observations
Latest: Form 483, Nov 5, 2013 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2013-11-05 | 483 Form 483 | San Jose, California | 15 | $99 |
Investigators on these documents
FEI number 3003434971 · most recent document Nov 5, 2013
About Leiter's Cambrian Park Drugs, Inc.
How many FDA Form 483s has Leiter's Cambrian Park Drugs, Inc. received?
FDA Intel has 1 Form 483 on file for Leiter's Cambrian Park Drugs, Inc.; the most recent is dated Nov 5, 2013.
When was Leiter's Cambrian Park Drugs, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Leiter's Cambrian Park Drugs, Inc. is a Form 483 dated Nov 5, 2013, for the site in San Jose, California.
What did FDA cite at Leiter's Cambrian Park Drugs, Inc.?
The regulations cited most in the observations on file for Leiter's Cambrian Park Drugs, Inc. are 21 CFR 211.42 (Design and construction features), 4 times; 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.192 (Production record review), 2 times.