Modern Products, Inc
FDA inspection history in Mequon, Wisconsin, 2001 to 2015
- 2
- Warning letters
- 1
- Form 483
Every document, by year
- Form 483
- Warning letter
2001: one warning letter; 2012: one warning letter; 2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2001One warning letter, at Mequon, Wisconsin.
- 2012One warning letter, at Mequon, Wisconsin.
- 2015One Form 483, at Mequon, Wisconsin.
Cited most
Across all Modern Products observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.137Expiration dating1
- 21 CFR 211.165Testing and release for distribution1
The complete Modern Products 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
Mequon, Wisconsin
Two warning letters and one Form 483 · 2001 to 2015 · 12 observations
Latest: Form 483, May 13, 2015 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-05-13 | 483 Form 483 | Mequon, Wisconsin | 12 | $99 |
| 2012-03-07 | Warning letter Warning letter | Mequon, Wisconsin | — | $99 |
| 2001-08-28 | Warning letter Warning letter | Mequon, Wisconsin | — | $99 |
Investigators on these documents
FEI number 2120711 · most recent document May 13, 2015
About Modern Products, Inc
How many FDA Form 483s has Modern Products, Inc received?
FDA Intel has 1 Form 483 on file for Modern Products, Inc; the most recent is dated May 13, 2015.
When was Modern Products, Inc last inspected by FDA?
The most recent FDA inspection document on file for Modern Products, Inc is a Form 483 dated May 13, 2015, for the site in Mequon, Wisconsin.
What did FDA cite at Modern Products, Inc?
The regulations cited most in the observations on file for Modern Products, Inc are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.113 (Control of microbiological contamination), 1 time.
Has Modern Products, Inc received an FDA warning letter?
Yes. FDA Intel has 2 FDA warning letters on file for Modern Products, Inc; the most recent is dated Mar 7, 2012.