FDA inspection

Heine Optotechnik Gmbh & Co. KG: FDA inspection ending Apr 29, 2010

FDA inspection 665813 · Voluntary Action Indicated (VAI) · GILCHING

Key facts

Inspection ID 665813
Firm Heine Optotechnik Gmbh & Co. KG
FEI number 1000379039
Address DORNIERSTR. 6
City GILCHING
Country Germany
Fiscal year 2010
Inspection end date Apr 29, 2010
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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