FDA Inspection 792669 — TechDevice LLC

TechDevice LLC — FEI 3003712030

The FDA completed an inspection of TechDevice LLC on Jul 31, 2012 in Watertown, MA. 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
Jul 31, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Watertown, MA (United States)