FDA Inspection 1100442 — Hummingbird Med Devices, Inc.

Hummingbird Med Devices, Inc. — FEI 3009382876

The FDA completed an inspection of Hummingbird Med Devices, Inc. on August 26, 2019 in Camano Island, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 26, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Camano Island, WA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures