FDA Inspection 695366 — Helena Laboratories, Inc

Helena Laboratories, Inc — FEI 1000116989

The FDA completed an inspection of Helena Laboratories, Inc on October 28, 2010 in Beaumont, TX. 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
October 28, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Beaumont, TX (United States)