FDA Inspection 1060874 — Osteotech, Inc.

Osteotech, Inc. — FEI 3002600221

The FDA completed an inspection of Osteotech, Inc. on July 30, 2018 in Eatontown, NJ. 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
July 30, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Eatontown, NJ (United States)