Form 483

Greer Laboratories, Inc. Form 483, 2017-06-15

FDA issued a Form 483 to Greer Laboratories, Inc. on 2017-06-15 with 14 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health14 observations

Greer Laboratories, Inc. · Lenoir, United States · Issued June 15, 2017

Overview

  • 14 public-safe observations are available for this inspection.
  • 7 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.

15 Jun 2017
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Gamal A Norton

15 Jun 2017
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Gamal A Norton

15 Jun 2017
21 CFR 820.120(b)

DHR documentation of label release {see also 820.184}

Cited by Gamal A Norton

15 Jun 2017
21 CFR 820.120(b)

DHR documentation of label release {see also 820.184}

Cited by Gamal A Norton

15 Jun 2017
21 CFR 820.181

DMR - not or inadequately maintained

Cited by Gamal A Norton

Inspected site

GLGreer Laboratories, Inc.Lenoir, 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 820.120(b)Cited across public-safe Form 483 observations2x
21 CFR 820.181Cited across public-safe Form 483 observations2x
21 CFR 820.184Cited across public-safe Form 483 observations2x
21 CFR 820.22Cited across public-safe Form 483 observations2x
21 CFR 820.75(a)Cited across public-safe Form 483 observations2x
21 CFR 820.80(d)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 14 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