Form 483

IodiTech, Inc. Form 483, 2017-07-13

FDA issued a Form 483 to IodiTech, Inc. on 2017-07-13 with 3 public-safe observations.

483· Form 483 issuedFoods & Cosmetics3 observations

IodiTech, Inc. · Kansas City, United States · Issued July 13, 2017

Overview

  • 3 public-safe observations are available for this inspection.
  • 1 structured CFR citation is represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

13 Jul 2017
21 CFR 211.84(d)(2)

Component identification test

Cited by Rita K Kabaso, Tristian E Strait

13 Jul 2017
21 CFR 211.84(d)(2)

Component identification test

Cited by Rita K Kabaso, Tristian E Strait

13 Jul 2017
21 CFR 211.84(d)(2)

Component identification test

Cited by Rita K Kabaso, Tristian E Strait

Inspected site

IIIodiTech, Inc.Kansas City, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.84(d)(2)Cited across public-safe Form 483 observations3x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 3 observations

The source PDF and 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