FDA inspection

RENISHAW MAYFIELD: FDA inspection ending Jul 21, 2016

FDA inspection 982423 · Voluntary Action Indicated (VAI) · Chassieu

Key facts

Inspection ID 982423
Firm RENISHAW MAYFIELD
FEI number 3009108888
Address 31 Rue Ampere
City Chassieu
Country France
Fiscal year 2016
Inspection end date Jul 21, 2016
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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