Form 483

EKOM spol. s.r.o. Form 483, 2024-03-21

FDA issued a Form 483 to EKOM spol. s.r.o. on 2024-03-21 with 3 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health3 observations

EKOM spol. s.r.o. · Piestany, Slovakia · Issued March 21, 2024

Overview

  • 3 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.

21 Mar 2024
21 CFR 820.184

DHR - not or inadequately maintained

Cited by John A Sciacchitano

21 Mar 2024
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by John A Sciacchitano

21 Mar 2024
21 CFR 820.72(b)

Remedial action

Cited by John A Sciacchitano

Inspected site

ESEKOM spol. s.r.o.Piestany, Slovakia

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.184Cited across public-safe Form 483 observations1x
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.72(b)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 3 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