FDA Inspection 1135596 — Corcept Therapeutics Incorporated

Corcept Therapeutics Incorporated — FEI 3005389393

The FDA completed an inspection of Corcept Therapeutics Incorporated on Oct 19, 2020 in Redwood City, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 19, 2020
Fiscal Year
2021
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Redwood City, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.