FDA Inspection 1110573 — Drucker Diagnostics

Drucker Diagnostics — FEI 3011765035

The FDA completed an inspection of Drucker Diagnostics on November 21, 2019 in Philipsburg, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 21, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Philipsburg, PA (United States)

Citations

IDCFRDescription
317021 CFR 820.198(b)Review and evaluation for investigation