# FDA Inspection 997378 - DNA Genotek Inc. - November 03, 2016

Source: https://www.keypedia.com/records/fda_inspections/dna-genotek-inc/7fa805de-ba15-4c3d-bcd7-c81d95d13ca2
Source feed: FDA_Inspections

> FDA Inspection 997378 for DNA Genotek Inc. on November 03, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 997378
- Company Name: DNA Genotek Inc.
- Inspection Date: 2016-11-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 997378 - 2016-11-03](https://www.keypedia.com/records/fda_inspections/dna-genotek-inc/752bb167-4c20-45cb-ab0c-2325a2e4011f)
- [FDA Inspection 851753 - 2013-09-20](https://www.keypedia.com/records/fda_inspections/dna-genotek-inc/480736ed-acbc-49b8-90f9-db36fd8d5a43)

Company: https://www.keypedia.com/companies/dna-genotek-inc/b40c2357-0700-4b9f-ad3a-975c25987eb7

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