Form 483

APS Materials, Inc. Form 483, 2016-03-03

FDA issued a Form 483 to APS Materials, Inc. on 2016-03-03 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

APS Materials, Inc. · Dayton, United States · Issued March 3, 2016

Overview

  • 3 public-safe observations are available for this inspection.
  • 3 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

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

3 Mar 2016
21 CFR 820.22

Quality audits - auditor independence

Cited by Cynthia T Cain, James G Marsh

3 Mar 2016
21 CFR 820.25(b)

Training - Lack of or inadequate procedures

Cited by Cynthia T Cain, James G Marsh

3 Mar 2016
21 CFR 820.40

Procedures not adequately established or maintained

Cited by Cynthia T Cain, James G Marsh

Inspected site

AMAPS Materials, Inc.Dayton, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.22Cited across public-safe Form 483 observations1x
21 CFR 820.25(b)Cited across public-safe Form 483 observations1x
21 CFR 820.40Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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