FDA Inspection 1123140 — Therapak LLC

Therapak LLC — FEI 3006450277

The FDA completed an inspection of Therapak LLC on March 2, 2020 in Buford, GA. 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
March 2, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Buford, GA (United States)