FDA Inspection 820394 — Affymax, Inc.

Affymax, Inc. — FEI 3009060530

The FDA completed an inspection of Affymax, Inc. on March 20, 2013 in Cupertino, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 20, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cupertino, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)