FDA Inspection 1243483 — Helios Biomedical
The FDA completed an inspection of Helios Biomedical on Jun 27, 2024 in Natick, MA. 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
- Jun 27, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Natick, MA (United States)