Jacobus Pharmaceutical Company, Inc.
FDA inspection history across 2 sites, 2011 to 2012
- 1
- Form 483
- 1
- Response
Every document, by year
- Form 483
- Response
2011: one 483 response; 2012: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2011–12One 483 response and one Form 483, at Princeton, New Jersey and Plainsboro, New Jersey.
Cited most
Across all Jacobus Pharmaceutical Company observations on file
- 21 CFR 211.105Equipment identification1
- 21 CFR 211.192Production record review1
- 21 CFR 211.42Design and construction features1
- 21 CFR 211.58Maintenance1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Jacobus Pharmaceutical Company file.
All 2 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
Plainsboro, New Jersey
One Form 483 · 2012 · 6 observations
Latest: Form 483, Apr 16, 2012 →Princeton, New Jersey
One 483 response · 2011
Latest: Response, Mar 9, 2011 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2012-04-16 | 483 Form 483 | Plainsboro, New Jersey | 6 | $99 |
| 2011-03-09 | Response 483 response | Princeton, New Jersey | — | $199 |
Investigators on these documents
FEI number 2343092 · most recent document Apr 16, 2012
About Jacobus Pharmaceutical Company, Inc.
How many FDA Form 483s has Jacobus Pharmaceutical Company, Inc. received?
FDA Intel has 1 Form 483 on file for Jacobus Pharmaceutical Company, Inc.; the most recent is dated Apr 16, 2012.
When was Jacobus Pharmaceutical Company, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Jacobus Pharmaceutical Company, Inc. is a Form 483 dated Apr 16, 2012, for the site in Plainsboro, New Jersey.
What did FDA cite at Jacobus Pharmaceutical Company, Inc.?
The regulations cited most in the observations on file for Jacobus Pharmaceutical Company, Inc. are 21 CFR 211.105 (Equipment identification), 1 time; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.42 (Design and construction features), 1 time.