FDA inspection

Etex Corporation: FDA inspection ending May 23, 2019

FDA inspection 1090850 · Voluntary Action Indicated (VAI) · Braintree, MA

Key facts

Inspection ID 1090850
Firm Etex Corporation
FEI number 3000206397
Address 55 Messina Dr
City Braintree
State MA
ZIP 02184
Country United States
Fiscal year 2019
Inspection end date May 23, 2019
Classification Voluntary Action Indicated (VAI)
Project area Blood and Blood Products
Product type Biologics

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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