FDA Inspection 1060870 — Hemostatix Medical Technologies LLC

Hemostatix Medical Technologies LLC — FEI 3006119098

The FDA completed an inspection of Hemostatix Medical Technologies LLC on February 2, 2018 in Bartlett, TN. 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
February 2, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bartlett, TN (United States)