FDA Inspection 876245 — Titronics Research & Development Co.

Titronics Research & Development Co. — FEI 3001451268

The FDA completed an inspection of Titronics Research & Development Co. on April 16, 2014 in Tiffin, IA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 16, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Tiffin, IA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
341521 CFR 820.22Quality Audit/Reaudit - conducted
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency