Clarcon Biological Chemistry Laboratory
FDA inspection history in Roy, Utah, 2009
- 1
- Form 483
Every document, by year
- Form 483
2009: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2009One Form 483, at Roy, Utah.
Cited most
Across all Clarcon Biological Chemistry Laboratory observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.105(a)Equipment identification1
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.130Packaging and labeling operations1
- 21 CFR 211.134Drug product inspection1
The complete Clarcon Biological Chemistry Laboratory file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Roy, Utah
One Form 483 · 2009 · 18 observations
Latest: Form 483, May 4, 2009 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2009-05-04 | 483 Form 483 | Roy, Utah | 18 | $99 |
Investigators on these documents
FEI number 3007026789 · most recent document May 4, 2009
About Clarcon Biological Chemistry Laboratory
How many FDA Form 483s has Clarcon Biological Chemistry Laboratory received?
FDA Intel has 1 Form 483 on file for Clarcon Biological Chemistry Laboratory; the most recent is dated May 4, 2009.
When was Clarcon Biological Chemistry Laboratory last inspected by FDA?
The most recent FDA inspection document on file for Clarcon Biological Chemistry Laboratory is a Form 483 dated May 4, 2009, for the site in Roy, Utah.
What did FDA cite at Clarcon Biological Chemistry Laboratory?
The regulations cited most in the observations on file for Clarcon Biological Chemistry Laboratory are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.105(a) (Equipment identification), 1 time; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time.