FDA Inspection 1058065 — Mooncup LTD
The FDA completed an inspection of Mooncup LTD on May 3, 2018 in Brighton. 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 3, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Brighton (United Kingdom)