FDA Inspection 922618 — Hologic, Inc.

Hologic, Inc. — FEI 2024800

The FDA completed an inspection of Hologic, Inc. on April 10, 2015 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
April 10, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
San Diego, CA (United States)

Additional Details

Postmarket Audit Inspections