FDA Inspection 967771 — Aggredyne, Inc.

Aggredyne, Inc. — FEI 3009610394

The FDA completed an inspection of Aggredyne, Inc. on April 5, 2016 in Houston, 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
April 5, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Houston, TX (United States)