FDA Inspection 895597 — Sechrist Industries Inc

Sechrist Industries Inc — FEI 2020676

The FDA completed an inspection of Sechrist Industries Inc on Sep 12, 2014 in Anaheim, CA. 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). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 12, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Anaheim, CA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
334621 CFR 820.200(b)Analyzing service report
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures