FDA Inspection 1238089 — RIO BIOFARMA BRASIL LTDA
The FDA completed an inspection of RIO BIOFARMA BRASIL LTDA on May 9, 2024 in Hortolandia. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- May 9, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hortolandia (Brazil)