FDA Inspection 718683 — Kedplasma LLC

Kedplasma LLC — FEI 3004158206

The FDA completed an inspection of Kedplasma LLC on April 8, 2011 in Temple Terrace, FL. 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
April 8, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Temple Terrace, FL (United States)