FDA Inspection 1305282 — Kimball Electronics - Indianapolis
The FDA completed an inspection of Kimball Electronics - Indianapolis on March 3, 2026 in Indianapolis, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- March 3, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Indianapolis, IN (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 23258 | ISO 13485:2016 Clause 8.5.2 | Corrective action procedures not documented |