FDA inspection

Cerovene Inc.: FDA inspection ending Nov 5, 2018

FDA inspection 1074159 · No Action Indicated (NAI) · Valley Cottage, NY

Key facts

Inspection ID 1074159
Firm Cerovene Inc.
FEI number 3005890568
Address 612 Corporate Way Ste 10
City Valley Cottage
State NY
ZIP 10989
Country United States
Fiscal year 2019
Inspection end date Nov 5, 2018
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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