# Covalon Technologies Ltd. – FDA Inspection, Jan 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/covalon-technologies-ltd/cc5db8e5-9a55-492c-ac9d-45a197988a4d
Source feed: FDA_Inspections

> FDA inspection 1039040 of Covalon Technologies Ltd., January 18, 2018. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1039040
- Company Name: Covalon Technologies Ltd.
- Inspection Date: 2018-01-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1132036 - 2018-09-12](https://www.keypedia.com/records/fda_inspections/covalon-technologies-ltd/82601112-c29d-46c2-addc-1de4d86b7e16)
- FDA Inspection 882734 - 2014-04-24

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

Company: https://www.keypedia.com/companies/covalon-technologies-ltd/41878779-a9e9-4a40-af70-8dfa89b7b42a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7