# FDA Inspection 1026019 - Integrated DNA Technologies, Inc - July 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/integrated-dna-technologies-inc/0eaa5d50-5b7e-4b78-88cf-1e0261e7aa4a
Source feed: FDA_Inspections

> FDA Inspection 1026019 for Integrated DNA Technologies, Inc on July 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026019
- Company Name: Integrated DNA Technologies, Inc
- Inspection Date: 2017-07-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1026019 - 2017-07-21](https://www.keypedia.com/records/fda_inspections/integrated-dna-technologies-inc/b8d7f906-d1ce-4bcd-b9c3-3ce8d666594b)
- [FDA Inspection 731006 - 2011-06-23](https://www.keypedia.com/records/fda_inspections/integrated-dna-technologies-inc/8aaa9148-b84a-4270-bce9-c65835f85309)

Company: https://www.keypedia.com/companies/integrated-dna-technologies-inc/0bedb765-744f-4a3b-8cae-5ce01eb883cc

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