Form 483

Shippert Medical Technologies Form 483, 2016-11-10

FDA issued a Form 483 to Shippert Medical Technologies on 2016-11-10 with 10 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health10 observations

Shippert Medical Technologies · Centennial, United States · Issued November 10, 2016

Overview

  • 10 public-safe observations are available for this inspection.
  • 5 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.

10 Nov 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Christine I Shaw

10 Nov 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Christine I Shaw

10 Nov 2016
21 CFR 820.30(d)

Design output - Lack of or inadequate procedures

Cited by Christine I Shaw

10 Nov 2016
21 CFR 820.30(d)

Design output - Lack of or inadequate procedures

Cited by Christine I Shaw

10 Nov 2016
21 CFR 820.30(i)

Design changes - Lack of or Inadequate Procedures

Cited by Christine I Shaw

Inspected site

SMShippert Medical TechnologiesCentennial, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.30(d)Cited across public-safe Form 483 observations2x
21 CFR 820.30(i)Cited across public-safe Form 483 observations2x
21 CFR 820.75(a)Cited across public-safe Form 483 observations2x
21 CFR 820.80(e)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 10 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