FDA Inspection 1085365 — Siemens Healthcare Diagnostics Inc.

Siemens Healthcare Diagnostics Inc. — FEI 3003932969

The FDA completed an inspection of Siemens Healthcare Diagnostics Inc. on March 18, 2019 in Berkeley, 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
March 18, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Berkeley, CA (United States)

Additional Details

Postmarket Audit Inspections