FDA Inspection 1111915 — Spera Nexus, Inc.

Spera Nexus, Inc. — FEI 3002807324

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