Form 483

Avazzia, Inc Form 483, 2017-08-30

FDA issued a Form 483 to Avazzia, Inc on 2017-08-30 with 6 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health6 observations

Avazzia, Inc · Dallas, United States · Issued August 30, 2017

Overview

  • 6 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.

30 Aug 2017
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Karen M Rodriguez

30 Aug 2017
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Karen M Rodriguez

30 Aug 2017
21 CFR 820.70(c)

Environmental control Lack of or inadequate procedures

Cited by Karen M Rodriguez

30 Aug 2017
21 CFR 820.70(c)

Environmental control Lack of or inadequate procedures

Cited by Karen M Rodriguez

30 Aug 2017
21 CFR 820.80(e)

Documentation

Cited by Karen M Rodriguez

Inspected site

AIAvazzia, IncDallas, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.50Cited across public-safe Form 483 observations2x
21 CFR 820.70(c)Cited across public-safe Form 483 observations2x
21 CFR 820.80(e)Cited across public-safe Form 483 observations2x

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