FDA Inspection 1195354 — Springboard Manufacturing
The FDA completed an inspection of Springboard Manufacturing on Jan 12, 2023 in South Bend, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 12, 2023
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- South Bend, IN (United States)