FDA Inspection 1021686 — Hilsinger Company Parent, LLC

Hilsinger Company Parent, LLC — FEI 1039131

The FDA completed an inspection of Hilsinger Company Parent, LLC on August 14, 2017 in Fairfield, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 14, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Fairfield, OH (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures