FDA Inspection 1078934 — Invotec International Inc.

Invotec International Inc. — FEI 1000113735

The FDA completed an inspection of Invotec International Inc. on Feb 5, 2019 in Jacksonville, FL. 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
Feb 5, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Jacksonville, FL (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
311921 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation