Agilent Technologies, Inc.
FDA inspection history in Santa Clara, California, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Santa Clara, California.
Cited most
Across all Agilent Technologies observations on file
- 21 CFR 820.120Device labeling1
- 21 CFR 820.198(a)Complaint files1
The complete Agilent Technologies file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Santa Clara, California
One Form 483 · 2015 · 2 observations
Latest: Form 483, Jul 6, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-07-06 | 483 Form 483 | Santa Clara, California | 2 | $99 |
Investigators on these documents
FEI number 2916205 · most recent document Jul 6, 2015
About Agilent Technologies, Inc.
How many FDA Form 483s has Agilent Technologies, Inc. received?
FDA Intel has 1 Form 483 on file for Agilent Technologies, Inc.; the most recent is dated Jul 6, 2015.
When was Agilent Technologies, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Agilent Technologies, Inc. is a Form 483 dated Jul 6, 2015, for the site in Santa Clara, California.
What did FDA cite at Agilent Technologies, Inc.?
The regulations cited most in the observations on file for Agilent Technologies, Inc. are 21 CFR 820.120 (Device labeling), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.