FDA Inspection 780115 — Neurotherm LLC

Neurotherm LLC — FEI 3002953813

The FDA completed an inspection of Neurotherm LLC on April 26, 2012 in Wilmington, MA. 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 26, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Wilmington, MA (United States)