FDA inspection

EKOM spol. s.r.o.: FDA inspection ending Mar 21, 2024

FDA inspection 1233666 · Voluntary Action Indicated (VAI) · Piestany

Key facts

Inspection ID 1233666
Firm EKOM spol. s.r.o.
FEI number 3005245901
Address Priemyselna 5031/18
City Piestany
Country Slovakia
Fiscal year 2024
Inspection end date Mar 21, 2024
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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