FDA inspection

SomnoMed Phillipines Inc.: FDA inspection ending Jan 28, 2016

FDA inspection 957017 · Voluntary Action Indicated (VAI) · Makati City

Key facts

Inspection ID 957017
Firm SomnoMed Phillipines Inc.
FEI number 3009440973
Address Allegro Center, Level 3, 2284 Pasong Tamo Ext.
City Makati City
Country Philippines
Fiscal year 2016
Inspection end date Jan 28, 2016
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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