FDA inspection

Bionik, Inc.: FDA inspection ending Feb 6, 2007

FDA inspection 460942 · No Action Indicated (NAI) · Watertown, MA

Key facts

Inspection ID 460942
Firm Bionik, Inc.
FEI number 3002758968
Address 80 Coolidge Hill Rd
City Watertown
State MA
ZIP 02472-5003
Fiscal year 2007
Inspection end date Feb 6, 2007
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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