FDA Inspection 951686 — Mid-Missouri Reproductive Med & Srgry Inc

Mid-Missouri Reproductive Med & Srgry Inc — FEI 3005172451

The FDA completed an inspection of Mid-Missouri Reproductive Med & Srgry Inc on Dec 1, 2015 in Columbia, MO. 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
Dec 1, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Columbia, MO (United States)