FDA Inspection 1117461 — Drucker Diagnostics

Drucker Diagnostics — FEI 3012519423

The FDA completed an inspection of Drucker Diagnostics on November 19, 2019 in Port Matilda, PA. 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
November 19, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Port Matilda, PA (United States)