FDA Inspection 699964 — Talisman Limited

Talisman Limited — FEI 3004585612

The FDA completed an inspection of Talisman Limited on November 18, 2010 in Leesburg, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 18, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Leesburg, VA (United States)