FDA Inspection 1025887 — Neotech Products, LLC

Neotech Products, LLC — FEI 2025917

The FDA completed an inspection of Neotech Products, LLC on August 10, 2017 in Valencia, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 10, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Valencia, CA (United States)