FDA inspection

ANJI ZHENGBANG MEDICAL INSTRUMENT CO, LTD: FDA inspection ending Jul 4, 2013

FDA inspection 841696 · Official Action Indicated (OAI) · Anji

Key facts

Inspection ID 841696
Firm ANJI ZHENGBANG MEDICAL INSTRUMENT CO, LTD
FEI number 3007738846
Address Tianhuangping, Anjixian
City Anji
Country China
Fiscal year 2013
Inspection end date Jul 4, 2013
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices
Warning letter 409682

At a glance

  • None Citations
  • 1–9 Posted citations
  • Yes 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

Browse all FDA inspections