FDA inspection

HT Co., Ltd.: FDA inspection ending Apr 18, 2013

FDA inspection 828085 · Voluntary Action Indicated (VAI) · Giheung-gu, Yongin-Si

Key facts

Inspection ID 828085
Firm HT Co., Ltd.
FEI number 3005256634
Address # 1313 Heungdeok Jungangno 120 U-Tower
City Giheung-gu, Yongin-Si
Country Korea (the Republic of)
Fiscal year 2013
Inspection end date Apr 18, 2013
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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