FDA Inspection 790399 — Apheresis Technologies, Inc.

Apheresis Technologies, Inc. — FEI 1000113717

The FDA completed an inspection of Apheresis Technologies, Inc. on July 13, 2012 in Palm Harbor, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 13, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Palm Harbor, FL (United States)

Citations

IDCFRDescription
315921 CFR 820.184DHR content
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
367821 CFR 820.30(g)Design Validation - Risk analysis not performed/inadequate