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FDA inspection

TWI Pharmaceuticals, Inc.: FDA inspection ending Dec 16, 2016

FDA inspection 998389 · Voluntary Action Indicated (VAI) · Taoyuan City

Key facts

Inspection ID 998389
Firm TWI Pharmaceuticals, Inc.
FEI number 3005674517
Address Zhongli Industrial Zone,Zhongli City, No. 3-1 Ziqiang 4th Rd.; Zhongli Dist.
City Taoyuan City
Fiscal year 2017
Inspection end date Dec 16, 2016
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation
Product type Devices, Drugs

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.

Other inspections at this establishment

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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