FDA Inspection 1005517 — Boekel Scientific

Boekel Scientific — FEI 3005953362

The FDA completed an inspection of Boekel Scientific on Mar 10, 2017 in Feasterville Trevose, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 10, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Feasterville Trevose, PA (United States)

Citations

IDCFRDescription
48621 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements