FDA Inspection 1089801 — Amalgam Rx, Inc.
The FDA completed an inspection of Amalgam Rx, Inc. on April 11, 2019 in Wilmington, DE. 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
- April 11, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Wilmington, DE (United States)