FDA inspection

Coopervision Manufacturing, Ltd.: FDA inspection ending Apr 15, 2010

FDA inspection 665657 · Voluntary Action Indicated (VAI) · Southampton

Key facts

Inspection ID 665657
Firm Coopervision Manufacturing, Ltd.
FEI number 3002806417
Address Unit 2, Hamble Court Business Park; Hamble Lane
City Southampton
Country United Kingdom
Fiscal year 2010
Inspection end date Apr 15, 2010
Classification Voluntary Action Indicated (VAI)
Project area Project Evaluation: 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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