# Canberra Corporation, Toledo, OH – FDA Inspections

Source: https://www.keypedia.com/companies/canberra-corporation/897a38d1-12e3-4b70-8e88-2bcc4eaf0fc6

> Inspection records and compliance data for Canberra Corporation in Toledo, Ohio. 5 FDA inspections on record, last inspected March 26, 2014.

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## Details

- Name: Canberra Corporation
- FEI Number: 1000508133
- Address Line 1: 3610 N Holland Sylvania Rd
- City: Toledo
- State: Ohio
- Zip Code: 43615
- Country Name: United States
- Address: 3610 N Holland Sylvania Rd, Toledo, Ohio 43615, United States
- Country: United States

## Related Documents

- [FDA Inspection 871450 - Canberra Corporation - 2014-03-26](https://www.keypedia.com/records/fda_inspections/canberra-corporation/4d5af0b3-a1ff-4a9b-aada-1fe63ca8601f) — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2014
- FDA Inspection 816541 - Canberra Corporation - 2013-02-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 21, 2013
- [FDA Inspection 816541 - Canberra Corporation - 2013-02-21](https://www.keypedia.com/records/fda_inspections/canberra-corporation/5a37867f-6e32-4061-a3c4-baee1061c23b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 21, 2013
- FDA Inspection 683537 - Canberra Corporation - 2010-09-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 14, 2010
- FDA Inspection 683537 - Canberra Corporation - 2010-09-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 14, 2010
- FDA Inspection 674022 - Canberra Corporation - 2010-08-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2010
- FDA Inspection 674022 - Canberra Corporation - 2010-08-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2010
- [FDA Inspection 648844 - Canberra Corporation - 2010-03-03](https://www.keypedia.com/records/fda_inspections/canberra-corporation/bc8dbc82-50d6-4db1-8541-e155e006981a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 3, 2010

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