FDA Inspection 897028 — Hyland LLC

Hyland LLC — FEI 3003616184

The FDA completed an inspection of Hyland LLC on Sep 24, 2014 in Bloomington, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 24, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Bloomington, MN (United States)