FDA inspection

Headstar Medical Products Co., Ltd.: FDA inspection ending Dec 15, 2016

FDA inspection 994816 · Voluntary Action Indicated (VAI) · New Taipei City

Key facts

Inspection ID 994816
Firm Headstar Medical Products Co., Ltd.
FEI number 3003418980
Address Wu Gu District, Hsin Chuan City, 7 Wugong 5th Rd.; Wugu Dist.
City New Taipei City
Country Taiwan
Fiscal year 2017
Inspection end date Dec 15, 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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