FDA Inspection 1192016 — Instylla, Inc.

Instylla, Inc. — FEI 3017208642

The FDA completed an inspection of Instylla, Inc. on November 16, 2022 in Bedford, MA. 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
November 16, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bedford, MA (United States)