FDA Inspection 1061444 — Surgical Direct, Inc.

Surgical Direct, Inc. — FEI 3003687489

The FDA completed an inspection of Surgical Direct, Inc. on August 3, 2018 in Orange City, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 3, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Orange City, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
312021 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures