# FDA Inspection 1108019 - Pretika Corporation - October 25, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/pretika-corporation/55227676-e61b-4807-bde3-d3dac736be92
Source feed: FDA_Inspections

> FDA Inspection 1108019 for Pretika Corporation on October 25, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1108019
- Company Name: Pretika Corporation
- Inspection Date: 2019-10-25
- 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 1108019 - 2019-10-25](https://www.globalkeysolutions.net/records/fda_inspections/pretika-corporation/3d7410bf-5066-49b6-9783-51834eb3a0fd)

Company: https://www.globalkeysolutions.net/companies/pretika-corporation/e6a13877-2cc1-43af-995e-4831da740a3a

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