FDA Inspection 1123129 — Elekta, Inc.
The FDA completed an inspection of Elekta, Inc. on December 13, 2019 in Atlanta, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- December 13, 2019
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Atlanta, GA (United States)