# Diversatek Healthcare – FDA Inspection, Jun 29, 2016

Source: https://www.keypedia.com/records/fda_inspections/diversatek-healthcare/97e0f1bf-53a5-48ff-a8cd-00b69eb644aa
Source feed: FDA_Inspections

> FDA inspection 977968 of Diversatek Healthcare, June 29, 2016. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 977968
- Company Name: Diversatek Healthcare
- Inspection Date: 2016-06-29
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1178591 - 2022-08-05
- [FDA Inspection 791104 - 2012-06-25](https://www.keypedia.com/records/fda_inspections/diversatek-healthcare/d2a253f4-70ec-46fb-b0b8-a28ce6be9b0f)
- FDA Inspection 584731 - 2009-03-20

Company: https://www.keypedia.com/companies/diversatek-healthcare/324fc552-0ff0-44f3-88a4-af2ffb065d70

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