3M Company
FDA inspection history in Saint Paul, Minnesota, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Saint Paul, Minnesota.
Cited most
Across all 3M observations on file
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160General requirements1
- 21 CFR 211.180General requirements1
The complete 3M file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Saint Paul, Minnesota
One Form 483 · 2015 · 3 observations
Latest: Form 483, Sep 1, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-09-01 | 483 Form 483 | Saint Paul, Minnesota | 3 | $99 |
Investigators on these documents
FEI number 3003803251 · most recent document Sep 1, 2015
About 3M Company
How many FDA Form 483s has 3M Company received?
FDA Intel has 1 Form 483 on file for 3M Company; the most recent is dated Sep 1, 2015.
When was 3M Company last inspected by FDA?
The most recent FDA inspection document on file for 3M Company is a Form 483 dated Sep 1, 2015, for the site in Saint Paul, Minnesota.
What did FDA cite at 3M Company?
The regulations cited most in the observations on file for 3M Company are 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.180 (General requirements), 1 time.