FDA Inspection 1022638 — ImpactLife
The FDA completed an inspection of ImpactLife on July 11, 2017 in Danville, IL. 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
- July 11, 2017
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Danville, IL (United States)