FDA inspection

Diopsys, Inc.: FDA inspection ending Mar 1, 2010

FDA inspection 651054 · Voluntary Action Indicated (VAI) · Middletown, PA

Key facts

Inspection ID 651054
Firm Diopsys, Inc.
FEI number 3004174467
Address 2 Wing Dr Ste 2A
City Middletown
State PA
ZIP 17057
Country United States
Fiscal year 2010
Inspection end date Mar 1, 2010
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 10–99 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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