Form 483

Bio-Detek, Inc. Form 483, 2017-10-25

FDA issued a Form 483 to Bio-Detek, Inc. on 2017-10-25 with 10 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health10 observations

Bio-Detek, Inc. · Pawtucket, United States · Issued October 25, 2017

Overview

  • 10 public-safe observations are available for this inspection.
  • 5 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.

25 Oct 2017
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Maryam Tabatabaie

25 Oct 2017
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Maryam Tabatabaie

25 Oct 2017
21 CFR 820.198(c)

Investigation of device failures

Cited by Maryam Tabatabaie

25 Oct 2017
21 CFR 820.198(c)

Investigation of device failures

Cited by Maryam Tabatabaie

25 Oct 2017
21 CFR 820.30(g)

Design validation - user needs and intended uses

Cited by Maryam Tabatabaie

Inspected site

BIBio-Detek, Inc.Pawtucket, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(a)Cited across public-safe Form 483 observations2x
21 CFR 820.198(c)Cited across public-safe Form 483 observations2x
21 CFR 820.30(g)Cited across public-safe Form 483 observations2x
21 CFR 820.75(a)Cited across public-safe Form 483 observations2x
21 CFR 820.80(a)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 10 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