FDA Inspection 1020164 — NEOORTHO PRODUTOS ORTOPEDICOS S/A
The FDA completed an inspection of NEOORTHO PRODUTOS ORTOPEDICOS S/A on May 18, 2017 in Curitiba. 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
- May 18, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Curitiba (Brazil)