FDA inspection

Gentell, Inc: FDA inspection ending Dec 12, 2019

FDA inspection 1112825 · Voluntary Action Indicated (VAI) · Bristol, PA

Key facts

Inspection ID 1112825
Firm Gentell, Inc
FEI number 1000522686
Address 2701 Bartram Rd
City Bristol
State PA
ZIP 19007
Country United States
Fiscal year 2020
Inspection end date Dec 12, 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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