FDA Inspection 1250621 — Etex Corporation

Etex Corporation — FEI 3000206397

The FDA completed an inspection of Etex Corporation on September 25, 2024 in Braintree, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 25, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Braintree, MA (United States)