FDA Inspection 1083980 — Ardelyx, Inc.

Ardelyx, Inc. — FEI 3010169178

The FDA completed an inspection of Ardelyx, Inc. on March 12, 2019 in Fremont, 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 12, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Fremont, CA (United States)

Additional Details

Sponsor, Contract Research Organization