FDA Inspection 1091481 — Med-Dyne, Inc.
The FDA completed an inspection of Med-Dyne, Inc. on May 21, 2019 in Louisville, KY. 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 21, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Louisville, KY (United States)