FDA Inspection 1110941 — Intermedic Arfran S.A.
The FDA completed an inspection of Intermedic Arfran S.A. on November 14, 2019 in Cerdanyola Del Valles. 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
- November 14, 2019
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Cerdanyola Del Valles (Spain)