FDA inspection

Etex Corporation: FDA inspection ending Sep 25, 2024

FDA inspection 1250621 · No Action Indicated (NAI) · Braintree, MA

Key facts

Inspection ID 1250621
Firm Etex Corporation
FEI number 3000206397
Address 55 Messina Dr
City Braintree
State MA
ZIP 02184
Country United States
Fiscal year 2024
Inspection end date Sep 25, 2024
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