FDA Inspection 1248801 — Mahana Therapeutics, Inc.

Mahana Therapeutics, Inc. — FEI 3017935596

The FDA completed an inspection of Mahana Therapeutics, Inc. on Aug 13, 2024 in San Francisco, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 13, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
San Francisco, CA (United States)