FDA Inspection 1010514 — Sparsha Pharma Usa Inc

Sparsha Pharma Usa Inc — FEI 3010888655

The FDA completed an inspection of Sparsha Pharma Usa Inc on April 28, 2017 in Oceanside, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
April 28, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Oceanside, CA (United States)