Nippon Sanso Matheson, Inc.
FDA inspection history in Bangor, Maine, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Bangor, Maine.
Cited most
Across all Nippon Sanso Matheson observations on file
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.89Rejected components, drug product containers, and closures1
The complete Nippon Sanso Matheson file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Bangor, Maine
One Form 483 · 2017 · 2 observations
Latest: Form 483, Apr 5, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-04-05 | 483 Form 483 | Bangor, Maine | 2 | $99 |
Investigators on these documents
FEI number 1221345 · most recent document Apr 5, 2017
About Nippon Sanso Matheson, Inc.
How many FDA Form 483s has Nippon Sanso Matheson, Inc. received?
FDA Intel has 1 Form 483 on file for Nippon Sanso Matheson, Inc.; the most recent is dated Apr 5, 2017.
When was Nippon Sanso Matheson, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Nippon Sanso Matheson, Inc. is a Form 483 dated Apr 5, 2017, for the site in Bangor, Maine.
What did FDA cite at Nippon Sanso Matheson, Inc.?
The regulations cited most in the observations on file for Nippon Sanso Matheson, Inc. are 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time; 21 CFR 211.89 (Rejected components, drug product containers, and closures), 1 time.