McNeil PPC, Inc.
FDA inspection history across 2 sites, 2008 to 2014
- 1
- Close-out
- 1
- EIR
- 1
- Form 483
Every document, by year
- Close-out
- EIR
- Form 483
2008: one inspection report and one Form 483; 2014: one close-out letter.
The story so far
Built from the dates and citations on the documents themselves.
- 2008One inspection report and one Form 483, at Parsippany, New Jersey.
- 2014One close-out letter, at Skillman, New Jersey.
Cited most
Across all McNeil PPC observations on file
- 21 CFR 820.100Corrective and preventive action2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.198Complaint files1
- 21 CFR 820.198Complaint files1
- 21 CFR 820.50Purchasing controls1
The complete McNeil PPC 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
Parsippany, New Jersey
One inspection report and one Form 483 · 2008 · 6 observations
Latest: EIR, Jul 31, 2008 →Skillman, New Jersey
One close-out letter · 2014
Latest: Close-out, May 22, 2014 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2014-05-22 | Close-out Close-out letter | Skillman, New Jersey | — | $99 |
| 2008-07-31 | EIR EIR | Parsippany, New Jersey | — | $550 |
| 2008-07-07 | 483 Form 483 | Parsippany, New Jersey | 6 | $99 |
Investigators on these documents
FEI number 2211583 · most recent document May 22, 2014
About McNeil PPC, Inc.
How many FDA Form 483s has McNeil PPC, Inc. received?
FDA Intel has 1 Form 483 on file for McNeil PPC, Inc.; the most recent is dated Jul 7, 2008.
When was McNeil PPC, Inc. last inspected by FDA?
The most recent FDA inspection document on file for McNeil PPC, Inc. is an establishment inspection report (EIR) dated Jul 31, 2008, for the site in Parsippany, New Jersey.
What did FDA cite at McNeil PPC, Inc.?
The regulations cited most in the observations on file for McNeil PPC, Inc. are 21 CFR 820.100 (Corrective and preventive action), 2 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.198 (Complaint files), 1 time.