Quincy Bioscience Manufacturing Inc.
FDA inspection history in Madison, Wisconsin, 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 Madison, Wisconsin.
Cited most
Across all Quincy Bioscience Manufacturing observations on file
- 21 CFR 1111
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.137(a)Expiration dating1
- 21 CFR 211.160(b)General requirements1
The complete Quincy Bioscience Manufacturing file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Madison, Wisconsin
One Form 483 · 2015 · 13 observations
Latest: Form 483, Mar 9, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-03-09 | 483 Form 483 | Madison, Wisconsin | 13 | $99 |
Investigators on these documents
FEI number 3006486156 · most recent document Mar 9, 2015
About Quincy Bioscience Manufacturing Inc.
How many FDA Form 483s has Quincy Bioscience Manufacturing Inc. received?
FDA Intel has 1 Form 483 on file for Quincy Bioscience Manufacturing Inc.; the most recent is dated Mar 9, 2015.
When was Quincy Bioscience Manufacturing Inc. last inspected by FDA?
The most recent FDA inspection document on file for Quincy Bioscience Manufacturing Inc. is a Form 483 dated Mar 9, 2015, for the site in Madison, Wisconsin.
What did FDA cite at Quincy Bioscience Manufacturing Inc.?
The regulations cited most in the observations on file for Quincy Bioscience Manufacturing Inc. are 21 CFR 111, 1 time; 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time.