FDA Inspection 922302 — Osypka Medtec Inc.
The FDA completed an inspection of Osypka Medtec Inc. on April 15, 2015 in Longmont, CO. 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 15, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Longmont, CO (United States)