FDA Inspection 1338648 — ImpactLife
The FDA completed an inspection of ImpactLife on Sep 23, 2026 in Dubuque, IA. 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
- Sep 23, 2026
- Fiscal Year
- 2026
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Dubuque, IA (United States)