FDA Inspection 809068 — TIDI Products, LLC

TIDI Products, LLC — FEI 2182318

The FDA completed an inspection of TIDI Products, LLC on Nov 27, 2012 in Neenah, WI. 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
Nov 27, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Neenah, WI (United States)

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