FDA Inspection 1101778 — Amcrest Industries LLC

Amcrest Industries LLC — FEI 3010413413

The FDA completed an inspection of Amcrest Industries LLC on August 5, 2019 in Houston, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 5, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Houston, TX (United States)