Form 483

NuVasive Inc Form 483, 2017-05-26

FDA issued a Form 483 to NuVasive Inc on 2017-05-26 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

NuVasive Inc · San Diego, United States · Issued May 26, 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.

26 May 2017
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Donna L Besone

26 May 2017
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Donna L Besone

26 May 2017
21 CFR 803.50(a)(1)

Report of Death or Serious Injury

Cited by Donna L Besone

26 May 2017
21 CFR 820.30(g)

Design validation- Lack of or inadequate procedures

Cited by Donna L Besone

26 May 2017
21 CFR 820.30(g)

Design validation- Lack of or inadequate procedures

Cited by Donna L Besone

Inspected site

NINuVasive IncSan Diego, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.50(a)(1)Cited across public-safe Form 483 observations3x
21 CFR 820.30(g)Cited across public-safe Form 483 observations3x

Full 483 report

Get the verbatim text of all 6 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