FDA Inspection 1029253 — Interplex Medical LLC
The FDA completed an inspection of Interplex Medical LLC on October 17, 2017 in Milford, OH. 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
- October 17, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Milford, OH (United States)