Becton Dickinson and Company
FDA inspection history in Sandy, Utah, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at Sandy, Utah.
Cited most
Across all Becton Dickinson and observations on file
- 21 CFR 211.192Production record review3
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160(a)General requirements1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 314.81(b)(1)(ii)Other postmarketing reports1
The complete Becton Dickinson and file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Sandy, Utah
One Form 483 · 2018 · 7 observations
Latest: Form 483, Dec 14, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-12-14 | 483 Form 483 | Sandy, Utah | 7 | $99 |
Investigators on these documents
FEI number 1710034 · most recent document Dec 14, 2018
About Becton Dickinson and Company
How many FDA Form 483s has Becton Dickinson and Company received?
FDA Intel has 1 Form 483 on file for Becton Dickinson and Company; the most recent is dated Dec 14, 2018.
When was Becton Dickinson and Company last inspected by FDA?
The most recent FDA inspection document on file for Becton Dickinson and Company is a Form 483 dated Dec 14, 2018, for the site in Sandy, Utah.
What did FDA cite at Becton Dickinson and Company?
The regulations cited most in the observations on file for Becton Dickinson and Company are 21 CFR 211.192 (Production record review), 3 times; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160(a) (General requirements), 1 time.