FDA inspection

Amplivox Ltd: FDA inspection ending Dec 14, 2023

FDA inspection 1224982 · Official Action Indicated (OAI) · Oxford

Key facts

Inspection ID 1224982
Firm Amplivox Ltd
FEI number 3003138182
Address 29-30 Station Field Est,Kidlington
City Oxford
Country United Kingdom
Fiscal year 2024
Inspection end date Dec 14, 2023
Classification Official Action Indicated (OAI)
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

Browse all FDA inspections