Morton Grove Pharmaceuticals, Inc.
FDA inspection history in Morton Grove, Illinois, 2014 to 2021
- 3
- Form 483s
Every document, by year
- Form 483
2014: one Form 483; 2019: one Form 483; 2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2014One Form 483, at Morton Grove, Illinois.
- 2019–21Two Form 483s, at Morton Grove, Illinois.
- 2019The longest 483 on file: 17 observations over 17 pages at Morton Grove, Illinois.
Cited most
Across all Morton Grove Pharmaceuticals observations on file
- 21 CFR 211.160General requirements7
- 21 CFR 211.192Production record review5
- 21 CFR 211.166Stability testing3
- 21 CFR 211.198Complaint files3
- 21 CFR 211.22Responsibilities of quality control unit3
The complete Morton Grove Pharmaceuticals file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Morton Grove, Illinois
Three Form 483s · 2014 to 2021 · 41 observations
Latest: Form 483, May 20, 2021 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-05-20 | 483 Form 483 | Morton Grove, Illinois | 12 | $99 |
| 2019-10-31 | 483 Form 483 | Morton Grove, Illinois | 17 | $99 |
| 2014-03-26 | 483 Form 483 | Morton Grove, Illinois | 12 | $99 |
Investigators on these documents
Arsen Karapetyan (1)Brian D. Nicholson (1)Justin A. Boyd (1)Linda F. Murphy (1)Michele L. Glendenning (1)Nibin Varghese (1)Sandra A. Boyd (1)Sarah E. Rhoades (1)
FEI number 1420913 · most recent document May 20, 2021
About Morton Grove Pharmaceuticals, Inc.
How many FDA Form 483s has Morton Grove Pharmaceuticals, Inc. received?
FDA Intel has 3 Form 483s on file for Morton Grove Pharmaceuticals, Inc.; the most recent is dated May 20, 2021.
When was Morton Grove Pharmaceuticals, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Morton Grove Pharmaceuticals, Inc. is a Form 483 dated May 20, 2021, for the site in Morton Grove, Illinois.
What did FDA cite at Morton Grove Pharmaceuticals, Inc.?
The regulations cited most in the observations on file for Morton Grove Pharmaceuticals, Inc. are 21 CFR 211.160 (General requirements), 7 times; 21 CFR 211.192 (Production record review), 5 times; 21 CFR 211.166 (Stability testing), 3 times.