FDA Inspection 596723 — Titronics Research & Development Co.

Titronics Research & Development Co. — FEI 3001451268

The FDA completed an inspection of Titronics Research & Development Co. on Jul 14, 2009 in Tiffin, IA. 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
Jul 14, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Tiffin, IA (United States)

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