FDA Inspection 1060374 — Hinson and Hale Medical Technologies, Inc.

Hinson and Hale Medical Technologies, Inc. — FEI 3009382775

The FDA completed an inspection of Hinson and Hale Medical Technologies, Inc. on July 26, 2018 in Wilkesboro, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 26, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Wilkesboro, NC (United States)

Citations

IDCFRDescription
243021 CFR 820.30(b)Design plans - Lack of or inadequate
316021 CFR 820.184Lack of or inadequate DHR procedures