FDA Inspection 1054772 — Arch - MedTorque Inc.
The FDA completed an inspection of Arch - MedTorque Inc. on May 15, 2018 in Kenosha, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- May 15, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Kenosha, WI (United States)