Greenfield Global USA Inc
FDA inspection history in Brookfield, Connecticut, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Brookfield, Connecticut.
Cited most
Across all Greenfield Global USA observations on file
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.166Stability testing1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Greenfield Global USA file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Brookfield, Connecticut
One Form 483 · 2022 · 6 observations
Latest: Form 483, Jan 18, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-01-18 | 483 Form 483 | Brookfield, Connecticut | 6 | $99 |
Investigators on these documents
FEI number 3004304444 · most recent document Jan 18, 2022
About Greenfield Global USA Inc
How many FDA Form 483s has Greenfield Global USA Inc received?
FDA Intel has 1 Form 483 on file for Greenfield Global USA Inc; the most recent is dated Jan 18, 2022.
When was Greenfield Global USA Inc last inspected by FDA?
The most recent FDA inspection document on file for Greenfield Global USA Inc is a Form 483 dated Jan 18, 2022, for the site in Brookfield, Connecticut.
What did FDA cite at Greenfield Global USA Inc?
The regulations cited most in the observations on file for Greenfield Global USA Inc are 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.198 (Complaint files), 1 time.