FDA Inspection 1111915 — Spera Nexus, Inc.

Spera Nexus, Inc. — FEI 3002807324

The FDA completed an inspection of Spera Nexus, Inc. on Nov 1, 2019 in Kakegawa. 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
Nov 1, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kakegawa (Japan)

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