FDA inspection

Wykle, Inc.: FDA inspection ending Nov 13, 2003

FDA inspection 302648 · Voluntary Action Indicated (VAI) · Carson City, NV

Key facts

Inspection ID 302648
Firm Wykle, Inc.
FEI number 2020703
Address 2222 College Pkwy
City Carson City
State NV
ZIP 89706-7980
Fiscal year 2004
Inspection end date Nov 13, 2003
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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