Form 483

Summit Medical Products, Inc. Form 483, 2010-09-24

FDA issued a Form 483 to Summit Medical Products, Inc. on 2010-09-24 with 2 public-safe observations.

483· Form 483 issued2 observations

Summit Medical Products, Inc. · Sandy, United States · Issued September 24, 2010

Overview

  • 2 public-safe observations are available for this inspection.
  • 2 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.

24 Sep 2010
21 CFR 820.75(c)

Process changes - review, evaluation and revalidation

Cited by James R Montero

24 Sep 2010
21 CFR 820.80(d)

Lack of or inadequate final acceptance procedures

Cited by James R Montero

Inspected site

SMSummit Medical Products, Inc.Sandy, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.75(c)Cited across public-safe Form 483 observations1x
21 CFR 820.80(d)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 2 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