FDA inspection

Coopervision Manufacturing, Ltd.: FDA inspection ending Sep 4, 2015

FDA inspection 943206 · No Action Indicated (NAI) · Southampton

Key facts

Inspection ID 943206
Firm Coopervision Manufacturing, Ltd.
FEI number 3002806417
Address Unit 2, Hamble Court Business Park; Hamble Lane
City Southampton
Country United Kingdom
Fiscal year 2015
Inspection end date Sep 4, 2015
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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