FDA Inspection 1316530 — INSTANOSIS INC

INSTANOSIS INC — FEI 3030897502

The FDA completed an inspection of INSTANOSIS INC on Apr 30, 2026 in King Of Prussia, PA. 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
Apr 30, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
King Of Prussia, PA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.