FDA inspection

Zhejiang Guobang Pharmaceutical Co., Ltd: FDA inspection ending Jul 13, 2018

FDA inspection 1067561 · No Action Indicated (NAI) · Shangyu

Key facts

Inspection ID 1067561
Firm Zhejiang Guobang Pharmaceutical Co., Ltd
FEI number 3008617115
Address No 6 Weiwu Road Hangzhou, Industrial Zone
City Shangyu
Fiscal year 2018
Inspection end date Jul 13, 2018
Classification No Action Indicated (NAI)
Project area Generic Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None 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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