FDA inspection

Lingraphicare America, Inc.: FDA inspection ending Nov 15, 2019

FDA inspection 1109991 · Voluntary Action Indicated (VAI) · Princeton, NJ

Key facts

Inspection ID 1109991
Firm Lingraphicare America, Inc.
FEI number 1000123978
Address 103 Carnegie Ctr Ste 104
City Princeton
State NJ
ZIP 08540
Country United States
Fiscal year 2020
Inspection end date Nov 15, 2019
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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