FDA Inspection 984418 — Spryson America Inc.

Spryson America Inc. — FEI 2519945

The FDA completed an inspection of Spryson America Inc. on April 14, 2016 in Pittsburgh, PA. 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
April 14, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Pittsburgh, PA (United States)