FDA Inspection 1216992 — Vastrax, Inc.

Vastrax, Inc. — FEI 3027615685

The FDA completed an inspection of Vastrax, Inc. on Aug 17, 2023 in Andover, MA. 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
Aug 17, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Andover, MA (United States)

Additional details

Sponsor, Contract Research Organization

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