FDA Inspection 1101596 — Surgisil, LLP

Surgisil, LLP — FEI 3006007116

The FDA completed an inspection of Surgisil, LLP on August 14, 2019 in Plano, TX. 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
August 14, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Plano, TX (United States)