Agilent Technologies, Inc.
FDA inspection history in Boulder, Colorado, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Boulder, Colorado.
Cited most
Across all Agilent Technologies observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.160General requirements1
The complete Agilent Technologies file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Boulder, Colorado
One Form 483 · 2019 · 3 observations
Latest: Form 483, Aug 2, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-08-02 | 483 Form 483 | Boulder, Colorado | 3 | $99 |
FEI number 3007057070 · most recent document Aug 2, 2019
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 Aug 2, 2019.
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 Aug 2, 2019, for the site in Boulder, Colorado.
What did FDA cite at Agilent Technologies, Inc.?
The regulations cited most in the observations on file for Agilent Technologies, Inc. are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time; 21 CFR 211.160 (General requirements), 1 time.