FDA Inspection 761843 — Beacon Kalamazoo

Beacon Kalamazoo — FEI 1870525

The FDA completed an inspection of Beacon Kalamazoo on Jan 4, 2012 in Kalamazoo, MI. 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
Jan 4, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Kalamazoo, MI (United States)