FDA Inspection 1067107 — Harbor Medtech, Inc.
The FDA completed an inspection of Harbor Medtech, Inc. on August 22, 2018 in Lake Forest, CA. 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
- August 22, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Lake Forest, CA (United States)