FDA inspection

Kronner Prototypes, Inc.: FDA inspection ending Apr 12, 2017

FDA inspection 1009807 · Voluntary Action Indicated (VAI) · Roseburg, OR

Key facts

Inspection ID 1009807
Firm Kronner Prototypes, Inc.
FEI number 3018984
Address 1443 Upper Cleveland Rapids Rd
City Roseburg
State OR
ZIP 97471
Country United States
Fiscal year 2017
Inspection end date Apr 12, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 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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