FDA inspection

Corning Incorporated Discovery Labware: FDA inspection ending Oct 30, 2019

FDA inspection 1114892 · No Action Indicated (NAI) · Durham, NC

Key facts

Inspection ID 1114892
Firm Corning Incorporated Discovery Labware
FEI number 1000110807
Address 1 Becton Cir
City Durham
State NC
ZIP 27712
Country United States
Fiscal year 2020
Inspection end date Oct 30, 2019
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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