FDA inspection

FLEXICARE LANKA (PVT) LTD: FDA inspection ending May 9, 2024

FDA inspection 1238859 · Voluntary Action Indicated (VAI) · Kalutara District

Key facts

Inspection ID 1238859
Firm FLEXICARE LANKA (PVT) LTD
FEI number 3017202422
Address Raigama, 382/X, Kumbuka Road
City Kalutara District
Country Sri Lanka
Fiscal year 2024
Inspection end date May 9, 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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