Atlas

Form 483

DHEF, Inc. Form 483, 2017-01-26

FDA issued a Form 483 to DHEF, Inc. on 2017-01-26 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

DHEF, Inc. · New Taipei City, Taiwan · Issued January 26, 2017

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

26 Jan 2017
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Dawn M Braswell

26 Jan 2017
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Dawn M Braswell

26 Jan 2017
21 CFR 820.30(g)

Design validation - Risk analysis

Cited by Dawn M Braswell

26 Jan 2017
21 CFR 820.40

Procedures not adequately established or maintained

Cited by Dawn M Braswell

Inspected site

DIDHEF, Inc.New Taipei City, Taiwan

Inspection team

DMDawn M Braswell

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x
21 CFR 820.40Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 observations

Every observation in full, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere