Form 483

Neurowave Systems Inc Form 483, 2015-02-03

FDA issued a Form 483 to Neurowave Systems Inc on 2015-02-03 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Neurowave Systems Inc · Beachwood, United States · Issued February 3, 2015

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.

3 Feb 2015
21 CFR 820.30(f)

Design verification - documentation

Cited by Benjamin J Dastoli

3 Feb 2015
21 CFR 820.30(g)

Design Validation - Risk analysis not performed/inadequate

Cited by Benjamin J Dastoli

3 Feb 2015
21 CFR 820.30(j)

Design history file

Cited by Benjamin J Dastoli

3 Feb 2015
21 CFR 820.75(a)

Lack of or inadequate process validation

Cited by Benjamin J Dastoli

Inspected site

NSNeurowave Systems IncBeachwood, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.30(f)Cited across public-safe Form 483 observations1x
21 CFR 820.30(g)Cited across public-safe Form 483 observations1x
21 CFR 820.30(j)Cited across public-safe Form 483 observations1x
21 CFR 820.75(a)Cited across public-safe Form 483 observations1x

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 4 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