FDA inspection

Misawa Medical Industry Co. Ltd. Headquarters): FDA inspection ending Mar 23, 2006

FDA inspection 423844 · No Action Indicated (NAI) · Edogawa

Key facts

Inspection ID 423844
Firm Misawa Medical Industry Co. Ltd. Headquarters)
FEI number 392
Address 7 Chome 17-6, Hirai
City Edogawa
Fiscal year 2006
Inspection end date Mar 23, 2006
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

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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