FDA Inspection 1174674 — PainTEQ, LLC

PainTEQ, LLC — FEI 3015341611

The FDA completed an inspection of PainTEQ, LLC on June 23, 2022 in Riverview, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 23, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Riverview, FL (United States)