FDA inspection

Kronner Prototypes, Inc.: FDA inspection ending Feb 4, 2013

FDA inspection 816972 · Official Action Indicated (OAI) · Roseburg, OR

Key facts

Inspection ID 816972
Firm Kronner Prototypes, Inc.
FEI number 3018984
Address 1443 Upper Cleveland Rapids Rd
City Roseburg
State OR
ZIP 97471
Country United States
Fiscal year 2013
Inspection end date Feb 4, 2013
Classification Official Action Indicated (OAI)
Project area Postmarket Assurance: Devices
Product type Devices
Warning letter 393572

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes 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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