Form 483

TELEMED Form 483, 2023-03-16

FDA issued a Form 483 to TELEMED on 2023-03-16 with 4 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health4 observations

TELEMED · Vilnius, Lithuania · Issued March 16, 2023

Overview

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

16 Mar 2023
21 CFR 820.100(b)

Documentation

Cited by John A Sciacchitano

16 Mar 2023
21 CFR 820.184

DHR - not or inadequately maintained

Cited by John A Sciacchitano

16 Mar 2023
21 CFR 820.20(c)

Management review - Lack of or inadequate procedures

Cited by John A Sciacchitano

16 Mar 2023
21 CFR 820.50(a)(3)

Acceptable supplier records, inadequate records

Cited by John A Sciacchitano

Inspected site

TTELEMEDVilnius, Lithuania

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.100(b)Cited across public-safe Form 483 observations1x
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.20(c)Cited across public-safe Form 483 observations1x
21 CFR 820.50(a)(3)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 observations

The full inspection record, as Atlas holds it, 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