FDA inspection

Interscope, Inc.: FDA inspection ending May 5, 2023

FDA inspection 1205347 · Voluntary Action Indicated (VAI) · Northbridge, MA

Key facts

Inspection ID 1205347
Firm Interscope, Inc.
FEI number 3011697028
Address 200 Commerce Dr
City Northbridge
State MA
ZIP 01534
Country United States
Fiscal year 2023
Inspection end date May 5, 2023
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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