# Pretika Corporation – FDA Inspection, Oct 25, 2019

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

> FDA inspection 1108019 of Pretika Corporation, October 25, 2019. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1108019
- Company Name: Pretika Corporation
- Inspection Date: 2019-10-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

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

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