FDA-Inspected Site

Physician Engineered Products, Inc.

5 FDA inspections are on record for Physician Engineered Products, Inc. in Fryeburg, United States.

Clean· No action indicated

Fryeburg, United States · Last updated July 10, 2026

Overview

  • 5 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2017-10-20.

At a glance

Inspections

5

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
18 Oct 2017 – 20 Oct 2017Medical Devices & Rad HealthClean
22 Jun 2015 – 23 Jun 2015Medical Devices & Rad Health483View 483 →
21 Dec 2011Not recordedClean
9 Oct 2008Not recordedClean
17 Jul 2007Not recordedClean

Observations on record

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

23 Jun 2015
21 CFR 820.184

DHR - not or inadequately maintained

Cited by Stephen C Smith

23 Jun 2015
21 CFR 820.22

Quality Audit/Reaudit - conducted

Cited by Stephen C Smith

23 Jun 2015
21 CFR 820.25(b)

Training records

Cited by Stephen C Smith

23 Jun 2015
21 CFR 820.30(g)

Design validation - simulated testing

Cited by Stephen C Smith

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.25(b)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Physician Engineered Products, Inc.'s 1 Form 483

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