FDA Inspection 1178329 — ImpactLife

ImpactLife — FEI 3019882186

The FDA completed an inspection of ImpactLife on Aug 24, 2022 in Decatur, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 24, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Decatur, IL (United States)