Form 483

Fuji Dynamics Limited Form 483, 2017-03-09

FDA issued a Form 483 to Fuji Dynamics Limited on 2017-03-09 with 12 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health12 observations

Fuji Dynamics Limited · Dong Guan, China · Issued March 9, 2017

Overview

  • 12 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.

9 Mar 2017
21 CFR 803.17

Lack of Written MDR Procedures

Cited by That Q Dang

9 Mar 2017
21 CFR 803.17

Lack of Written MDR Procedures

Cited by That Q Dang

9 Mar 2017
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by That Q Dang

9 Mar 2017
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by That Q Dang

9 Mar 2017
21 CFR 820.100(b)

Documentation

Cited by That Q Dang

Inspected site

FDFuji Dynamics LimitedDong Guan, China

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 803.17Cited across public-safe Form 483 observations2x
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.100(b)Cited across public-safe Form 483 observations2x
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.198(b)Cited across public-safe Form 483 observations2x
21 CFR 820.25(b)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 12 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