# FDA Inspection 733356 - Diversatek Healthcare - July 06, 2011

Source: https://www.keypedia.com/records/fda_inspections/diversatek-healthcare/58e47fc3-5abb-41cf-afd5-a843372f6027
Source feed: FDA_Inspections

> FDA Inspection 733356 for Diversatek Healthcare on July 06, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 733356
- Company Name: Diversatek Healthcare
- Inspection Date: 2011-07-06
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 887415 - 2014-07-21](https://www.keypedia.com/records/fda_inspections/diversatek-healthcare/c7c80df1-9849-4299-8a56-04a7500a57f3)
- [FDA Inspection 733356 - 2011-07-06](https://www.keypedia.com/records/fda_inspections/diversatek-healthcare/70bba044-bf3a-4216-8f84-5bc4f0f4517c)

Company: https://www.keypedia.com/companies/diversatek-healthcare/1a32ae8e-a520-4ffb-90d4-9be4f5270f4f

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