FDA Inspection 891810 — Etex Corporation

Etex Corporation — FEI 3000206397

The FDA completed an inspection of Etex Corporation on August 19, 2014 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
August 19, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Braintree, MA (United States)