FDA Inspection 761829 — Lenstec, Inc.

Lenstec, Inc. — FEI 3001659659

The FDA completed an inspection of Lenstec, Inc. on Jan 24, 2012 in St Petersburg, FL. 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
Jan 24, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
St Petersburg, FL (United States)