FDA Inspection 858926 — Tactile Systems Technology, Inc.

Tactile Systems Technology, Inc. — FEI 3004183730

The FDA completed an inspection of Tactile Systems Technology, Inc. on Oct 29, 2013 in New Brighton, MN. 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
Oct 29, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
New Brighton, MN (United States)