FDA-Inspected Site

Enercon

2 FDA inspections are on record for Enercon in Gray, United States.

Clean· No action indicated

Gray, United States · Last updated July 9, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2023-04-19.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
17 Apr 2023 – 19 Apr 2023Medical Devices & Rad HealthClean
1 Aug 2017 – 3 Aug 2017Medical Devices & Rad Health483View 483 →

Observations on record

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

3 Aug 2017
21 CFR 820.90(a)

Nonconforming product, Lack of or inadequate procedures

Cited by James W Whitney, Jason B Prosser

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 820.90(a)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Enercon'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