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FDA Inspection 711692 — Biowave Corporation

Biowave Corporation — FEI 3004558433

The FDA completed an inspection of Biowave Corporation on February 18, 2011 in Westport, CT. 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
February 18, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Westport, CT (United States)

Facility

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