Form 483

Kalitec Direct, LLC Form 483, 2020-03-04

FDA issued a Form 483 to Kalitec Direct, LLC on 2020-03-04 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

Kalitec Direct, LLC · Oviedo, United States · Issued March 4, 2020

Overview

  • 4 public-safe observations are available for this inspection.
  • 2 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.

4 Mar 2020
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Richard K Vogel

4 Mar 2020
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Richard K Vogel

4 Mar 2020
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Richard K Vogel

4 Mar 2020
21 CFR 820.50

Purchasing controls, Lack of or inadequate procedures

Cited by Richard K Vogel

Inspected site

KDKalitec Direct, LLCOviedo, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations2x
21 CFR 820.50Cited across public-safe Form 483 observations2x

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 4 observations

The source PDF, 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