Form 483

JW North America, Inc. Form 483, 2017-09-22

FDA issued a Form 483 to JW North America, Inc. on 2017-09-22 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

JW North America, Inc. · Rockland, United States · Issued September 22, 2017

Overview

  • 6 public-safe observations are available for this inspection.
  • 2 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.

22 Sep 2017
21 CFR 820.30(a)

Design control - no procedures

Cited by John A Sciacchitano

22 Sep 2017
21 CFR 820.30(a)

Design control - no procedures

Cited by John A Sciacchitano

22 Sep 2017
21 CFR 820.30(a)

Design control - no procedures

Cited by John A Sciacchitano

22 Sep 2017
21 CFR 820.50(a)(2)

Supplier oversight

Cited by John A Sciacchitano

22 Sep 2017
21 CFR 820.50(a)(2)

Supplier oversight

Cited by John A Sciacchitano

Inspected site

JNJW North America, Inc.Rockland, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.30(a)Cited across public-safe Form 483 observations3x
21 CFR 820.50(a)(2)Cited across public-safe Form 483 observations3x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 6 observations

The source PDF and 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