FDA Inspection 1040490 — Agnieszka Nohawica

Agnieszka Nohawica — FEI 3014022703

The FDA completed an inspection of Agnieszka Nohawica on January 16, 2018 in Dalkeith. 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
January 16, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Dalkeith (United Kingdom)

Additional Details

Clinical Investigator (CI)