FDA inspection

Bushnell Inc: FDA inspection ending Apr 5, 2007

FDA inspection 468558 · No Action Indicated (NAI) · Overland Park, KS

Key facts

Inspection ID 468558
Firm Bushnell Inc
FEI number 2081037
Address 9200 Cody St
City Overland Park
State KS
ZIP 66214-1734
Fiscal year 2007
Inspection end date Apr 5, 2007
Classification No Action Indicated (NAI)
Project area Rad Cntrl & Hlth Safety Act (RCHSA) Auth
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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