FDA Inspection 1150237 — Osteotech, Inc.

Osteotech, Inc. — FEI 3002600221

The FDA completed an inspection of Osteotech, Inc. on August 12, 2021 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
August 12, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Eatontown, NJ (United States)