Form 483

iCRco, Inc. Form 483, 2018-04-20

FDA issued a Form 483 to iCRco, Inc. on 2018-04-20 with 12 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health12 observations

iCRco, Inc. · Goleta, United States · Issued April 20, 2018

Overview

  • 12 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.

20 Apr 2018
21 CFR 820.120

Lack of or inadequate procedures for labeling

Cited by Janet Pulver

20 Apr 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Janet Pulver

20 Apr 2018
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Janet Pulver

20 Apr 2018
21 CFR 820.72(a)

Calibration, Inspection, etc. Procedures Lack of or Inadequ

Cited by Janet Pulver

20 Apr 2018
21 CFR 820.72(a)

Calibration, Inspection, etc. Procedures Lack of or Inadequ

Cited by Janet Pulver

Inspected site

IIiCRco, Inc.Goleta, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.120Cited across public-safe Form 483 observations3x
21 CFR 820.198(a)Cited across public-safe Form 483 observations3x
21 CFR 820.72(a)Cited across public-safe Form 483 observations3x
21 CFR 820.80(b)Cited across public-safe Form 483 observations3x

Full 483 report

Get the verbatim text of all 12 observations

The full inspection record, as Atlas holds it, 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