FDA Inspection 755901 — Alliqua Biomedical

Alliqua Biomedical — FEI 3004052050

The FDA completed an inspection of Alliqua Biomedical on December 6, 2011 in Langhorne, PA. 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
December 6, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Langhorne, PA (United States)