FDA Inspection 677299 — Hemagen Diagnostics Inc

Hemagen Diagnostics Inc — FEI 1181055

The FDA completed an inspection of Hemagen Diagnostics Inc on August 25, 2010 in Baltimore, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 25, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Baltimore, MD (United States)