FDA Inspection 1181654 — Gredale, LLC

Gredale, LLC — FEI 3016711507

The FDA completed an inspection of Gredale, LLC on Sep 20, 2022 in Los Angeles, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 20, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Los Angeles, CA (United States)