Form 483

Splintek, Inc Form 483, 2016-02-05

FDA issued a Form 483 to Splintek, Inc on 2016-02-05 with 8 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health8 observations

Splintek, Inc · Lenexa, United States · Issued February 5, 2016

Overview

  • 8 public-safe observations are available for this inspection.
  • 3 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.

5 Feb 2016
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Jonathan R Campos

5 Feb 2016
21 CFR 803.17

Lack of Written MDR Procedures

Cited by Jonathan R Campos

5 Feb 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Jonathan R Campos

5 Feb 2016
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Jonathan R Campos

5 Feb 2016
21 CFR 820.198(a)

Complaints

Cited by Jonathan R Campos

Inspected site

SISplintek, IncLenexa, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations4x
21 CFR 803.17Cited across public-safe Form 483 observations2x
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 8 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