FDA Inspection 1148512 — Henke Sass Wolf Of America,Inc

Henke Sass Wolf Of America,Inc — FEI 1000120548

The FDA completed an inspection of Henke Sass Wolf Of America,Inc on Aug 11, 2021 in Dudley, MA. 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
Aug 11, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Dudley, MA (United States)

Citations

IDCFRDescription
316021 CFR 820.184Lack of or inadequate DHR procedures

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