Putney Inc.
FDA inspection history in Portland, 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 Portland, Maine.
Cited most
Across all Putney observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(a)Responsibilities of quality control unit1
The complete Putney file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Portland, Maine
One Form 483 · 2017 · 2 observations
Latest: Form 483, Mar 9, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-03-09 | 483 Form 483 | Portland, Maine | 2 | $99 |
Investigators on these documents
FEI number 3007299556 · most recent document Mar 9, 2017
About Putney Inc.
How many FDA Form 483s has Putney Inc. received?
FDA Intel has 1 Form 483 on file for Putney Inc.; the most recent is dated Mar 9, 2017.
When was Putney Inc. last inspected by FDA?
The most recent FDA inspection document on file for Putney Inc. is a Form 483 dated Mar 9, 2017, for the site in Portland, Maine.
What did FDA cite at Putney Inc.?
The regulations cited most in the observations on file for Putney Inc. are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22(a) (Responsibilities of quality control unit), 1 time.