FDA inspection

CorneaGen, LLC: FDA inspection ending Jul 20, 2018

FDA inspection 1061992 · No Action Indicated (NAI) · Winston Salem, NC

Key facts

Inspection ID 1061992
Firm CorneaGen, LLC
FEI number 3005357288
Address 101 N Chestnut St Ste 303
City Winston Salem
State NC
ZIP 27101
Country United States
Fiscal year 2018
Inspection end date Jul 20, 2018
Classification No Action Indicated (NAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

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

Browse all FDA inspections