FDA Inspection 1220574 — HertART ApS
The FDA completed an inspection of HertART ApS on August 28, 2023 in Vastra Frolunda. 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
- August 28, 2023
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Vastra Frolunda (Sweden)