FDA inspection

Brightway Holdings SDN BHD: FDA inspection ending Mar 21, 2013

FDA inspection 827442 · Voluntary Action Indicated (VAI) · Klang

Key facts

Inspection ID 827442
Firm Brightway Holdings SDN BHD
FEI number 1000153304
Address Lot 1559, 1 Jalan Istimewa, BATU BELAH
City Klang
Country Malaysia
Fiscal year 2013
Inspection end date Mar 21, 2013
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None 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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