FDA Inspection 851968 — Teratech Corporation

Teratech Corporation — FEI 3002315840

The FDA completed an inspection of Teratech Corporation on Aug 28, 2013 in Burlington, 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
Aug 28, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Burlington, MA (United States)