FDA Inspection 1115148 — Regalabs

Regalabs — FEI 1000305426

The FDA completed an inspection of Regalabs on November 12, 2019 in Canton, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 12, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Canton, GA (United States)