FDA Inspection 1065644 — Haemopharm Biofluids S.R.L.
The FDA completed an inspection of Haemopharm Biofluids S.R.L. on Jul 27, 2018 in Tovo Di Sant' Agata. 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
- Jul 27, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tovo Di Sant' Agata (Italy)