FDA Inspection 831783 — Jensen Industries, Inc.

Jensen Industries, Inc. — FEI 1219645

The FDA completed an inspection of Jensen Industries, Inc. on May 9, 2013 in North Haven, CT. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 9, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
North Haven, CT (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures