# Titronics Research & Development Co. - Inspection Records

Source: https://www.keypedia.com/companies/titronics-research-development-co/cb427513-a4b3-446a-8433-8053761a4f21

> Inspection records and compliance data for Titronics Research & Development Co. in Tiffin, Iowa. Access full analysis and detailed observations.

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## Details

- Name: Titronics Research & Development Co.
- FEI Number: 3001451268
- City: Tiffin
- State: Iowa
- Country Name: United States
- Address Line 1: 400 Stephans St Ste D
- Zip Code: 52340

## Related Documents

- [483 - Titronics Research & Development Co. - 2019-07-09](https://www.keypedia.com/records/483/titronics-research-development-co/12f3cb54-531d-4b90-bfb1-a57a3f10ea69) — source: FDA, date: July 9, 2019
- [FDA Inspection 1095737 - Titronics Research & Development Co. - 2019-07-09](https://www.keypedia.com/records/fda_inspections/titronics-research-development-co/0f6c343a-9e77-4f81-be34-05ccb5e2a8db) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 9, 2019
- [FDA Inspection 1095737 - Titronics Research & Development Co. - 2019-07-09](https://www.keypedia.com/records/fda_inspections/titronics-research-development-co/9595756a-b289-4b86-9994-e6a2d7e5e7d1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 9, 2019
- [FDA Inspection 876245 - Titronics Research & Development Co. - 2014-04-16](https://www.keypedia.com/records/fda_inspections/titronics-research-development-co/d0694974-3fd3-4465-9ea7-6e181809fca0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 16, 2014
- [FDA Inspection 876245 - Titronics Research & Development Co. - 2014-04-16](https://www.keypedia.com/records/fda_inspections/titronics-research-development-co/cfc3fc77-eac4-4b13-9f3f-728808cc6d2f) — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2014
- [FDA Inspection 596723 - Titronics Research & Development Co. - 2009-07-14](https://www.keypedia.com/records/fda_inspections/titronics-research-development-co/ffb4bc64-e95a-4a86-a9b8-555e2f86ccc3) — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2009

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