FDA Inspection 1256176 — Tetracore, Inc.

Tetracore, Inc. — FEI 3003517954

The FDA completed an inspection of Tetracore, Inc. on December 5, 2024 in Rockville, MD. 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
December 5, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Rockville, MD (United States)