FDA Inspection 1097095 — LUMA THERAPEUTICS

LUMA THERAPEUTICS — FEI 3013121317

The FDA completed an inspection of LUMA THERAPEUTICS on June 27, 2019 in Millbrae, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 27, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Millbrae, CA (United States)