FDA inspection

GFA Production Xiamen Co., Ltd.: FDA inspection ending Nov 7, 2014

FDA inspection 909122 · No Action Indicated (NAI) · Xiamen

Key facts

Inspection ID 909122
Firm GFA Production Xiamen Co., Ltd.
FEI number 3008384335
Address Huli Industrial Park, Tong'an District, 20 Meixi Avenue
City Xiamen
Country China
Fiscal year 2015
Inspection end date Nov 7, 2014
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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