FDA Inspection 900341 — Sunrise Medical Laboratories, Inc.

Sunrise Medical Laboratories, Inc. — FEI 3005372272

The FDA completed an inspection of Sunrise Medical Laboratories, Inc. on October 14, 2014 in Hicksville, NY. 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
October 14, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Hicksville, NY (United States)