FDA Inspection 1117794 — Osypka Medtec Inc.

Osypka Medtec Inc. — FEI 3010376846

The FDA completed an inspection of Osypka Medtec Inc. on January 31, 2020 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
January 31, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Longmont, CO (United States)