FDA Inspection 732047 — Biomet North Central

Biomet North Central — FEI 3006444006

The FDA completed an inspection of Biomet North Central on Jun 28, 2011 in Bloomington, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 28, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Bloomington, MN (United States)