Form 483

Caretaker Medical, Inc. Form 483, 2018-10-23

FDA issued a Form 483 to Caretaker Medical, Inc. on 2018-10-23 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Caretaker Medical, Inc. · Charlottesville, United States · Issued October 23, 2018

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.

23 Oct 2018
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Tiki Dixon

23 Oct 2018
21 CFR 820.120

Lack of or inadequate procedures for labeling

Cited by Tiki Dixon

23 Oct 2018
21 CFR 820.30(i)

Design changes - Lack of or Inadequate Procedures

Cited by Tiki Dixon

23 Oct 2018
21 CFR 820.70(b)

Production and Process Change Procedures, lack of or Inad.

Cited by Tiki Dixon

Inspected site

CMCaretaker Medical, Inc.Charlottesville, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17Cited across public-safe Form 483 observations1x
21 CFR 820.120Cited across public-safe Form 483 observations1x
21 CFR 820.30(i)Cited across public-safe Form 483 observations1x
21 CFR 820.70(b)Cited 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