FDA Inspection 807153 — Medalliance, Inc

Medalliance, Inc — FEI 3004123225

The FDA completed an inspection of Medalliance, Inc on Nov 14, 2012 in Glenside, PA. 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
Nov 14, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Glenside, PA (United States)

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