FDA Inspection 1252605 — Hologic, Inc.

Hologic, Inc. — FEI 2024800

The FDA completed an inspection of Hologic, Inc. on August 13, 2024 in San Diego, 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
August 13, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)