Goodwin Biotechnology, Inc
FDA inspection history in Plantation, Florida, 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 Plantation, Florida.
Cited most
Across all Goodwin Biotechnology observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 610.12Sterility1
The complete Goodwin Biotechnology file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Plantation, Florida
One Form 483 · 2019 · 3 observations
Latest: Form 483, Apr 10, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-04-10 | 483 Form 483 | Plantation, Florida | 3 | $99 |
Investigators on these documents
FEI number 3001861303 · most recent document Apr 10, 2019
About Goodwin Biotechnology, Inc
How many FDA Form 483s has Goodwin Biotechnology, Inc received?
FDA Intel has 1 Form 483 on file for Goodwin Biotechnology, Inc; the most recent is dated Apr 10, 2019.
When was Goodwin Biotechnology, Inc last inspected by FDA?
The most recent FDA inspection document on file for Goodwin Biotechnology, Inc is a Form 483 dated Apr 10, 2019, for the site in Plantation, Florida.
What did FDA cite at Goodwin Biotechnology, Inc?
The regulations cited most in the observations on file for Goodwin Biotechnology, Inc are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 610.12 (Sterility), 1 time.