Form 483

ALLY MEDICAL SUPPLIES Form 483, 2016-03-30

FDA issued a Form 483 to ALLY MEDICAL SUPPLIES on 2016-03-30 with 20 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health20 observations

ALLY MEDICAL SUPPLIES · Lakewood, United States · Issued March 30, 2016

Overview

  • 20 public-safe observations are available for this inspection.
  • 5 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

30 Mar 2016
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Melissa A Freeman, Doreen P Gubbay

30 Mar 2016
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Melissa A Freeman, Doreen P Gubbay

30 Mar 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Melissa A Freeman, Doreen P Gubbay

30 Mar 2016
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Melissa A Freeman, Doreen P Gubbay

30 Mar 2016
21 CFR 820.30(i)

Design changes - Lack of or Inadequate Procedures

Cited by Melissa A Freeman, Doreen P Gubbay

Inspected site

AMALLY MEDICAL SUPPLIESLakewood, 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 observations4x
21 CFR 820.198(a)Cited across public-safe Form 483 observations4x
21 CFR 820.30(i)Cited across public-safe Form 483 observations4x
21 CFR 820.50Cited across public-safe Form 483 observations4x
21 CFR 820.80(b)Cited across public-safe Form 483 observations4x

Full 483 report

Get the verbatim text of all 20 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