FDA Inspection 959188 — Mooncup LTD
The FDA completed an inspection of Mooncup LTD on January 27, 2016 in Brighton. 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
- January 27, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Brighton (United Kingdom)