FDA-Inspected Site

Putney Inc.

2 FDA inspections are on record for Putney Inc. in Portland, United States.

483· Form 483 issued

Portland, United States · Last updated August 15, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2017-03-09.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
27 Feb 2017 – 9 Mar 2017Human Drugs483View 483 →
28 Jun 2012Not recordedClean

Observations on record

Form 483 observations cited at this site, most recent first.

9 Mar 2017
21 CFR 211.192

Investigations of discrepancies, failures

Cited by John P Mistler, Erik W Koester

9 Mar 2017
21 CFR 211.192

Investigations of discrepancies, failures

Cited by John P Mistler, Erik W Koester

9 Mar 2017
21 CFR 211.22(a)

Contract drug products--lack of responsibility

Cited by John P Mistler, Erik W Koester

9 Mar 2017
21 CFR 211.22(a)

Contract drug products--lack of responsibility

Cited by John P Mistler, Erik W Koester

9 Mar 2017
21 CFR 211.25(a)

GMP Training Frequency

Cited by John P Mistler, Erik W Koester

Investigators

FDA investigators tied to this site in the record.

Ellen P Madigan1 insp.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 211.192Cited across public-safe Form 483 observations2x
21 CFR 211.22(a)Cited across public-safe Form 483 observations2x
21 CFR 211.25(a)Cited across public-safe Form 483 observations2x

Full site report

Get the verbatim findings behind Putney Inc.'s 1 Form 483

Source PDFs, verbatim observations, and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat