Form 483

Tokyo Boeki Medisys, Inc. Form 483, 2017-03-24

FDA issued a Form 483 to Tokyo Boeki Medisys, Inc. on 2017-03-24 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Tokyo Boeki Medisys, Inc. · Hino, Japan · Issued March 24, 2017

Overview

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

24 Mar 2017
21 CFR 803.17(a)(1)

Lack of System for Event Evaluations

Cited by Catherine J Laufmann

24 Mar 2017
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Catherine J Laufmann

24 Mar 2017
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Catherine J Laufmann

24 Mar 2017
21 CFR 820.250(b)

Sampling methods - Lack of or inadequate procedures

Cited by Catherine J Laufmann

24 Mar 2017
21 CFR 820.30(f)

Design verification - documentation

Cited by Catherine J Laufmann

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 820.100(a)Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.250(b)Cited across public-safe Form 483 observations1x
21 CFR 820.30(f)Cited across public-safe Form 483 observations1x
21 CFR 820.72(a)Cited across public-safe Form 483 observations1x

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