FDA Inspection 557515 — Tepha Incorporated

Tepha Incorporated — FEI 3005670760

The FDA completed an inspection of Tepha Incorporated on Oct 31, 2008 in Lexington, 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
Oct 31, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lexington, MA (United States)