# FDA Inspection 1117542 - Phamatech - January 23, 2020

Source: https://www.globalkeysolutions.net/records/fda_inspections/phamatech/7a4e16fb-a7c1-44de-9080-a0f3db7adb28
Source feed: FDA_Inspections

> FDA Inspection 1117542 for Phamatech on January 23, 2020. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1117542
- Company Name: Phamatech
- Inspection Date: 2020-01-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1262990 - 2025-02-11](https://www.globalkeysolutions.net/records/fda_inspections/phamatech/eca09a5d-fb02-44d3-a169-50d989669db2)
- [FDA Inspection 1194665 - 2022-12-15](https://www.globalkeysolutions.net/records/fda_inspections/phamatech/9c93bf7b-2954-4104-b069-2bc1a23d9f84)
- [FDA Inspection 1194665 - 2022-12-15](https://www.globalkeysolutions.net/records/fda_inspections/phamatech/f7764c72-894f-472b-97be-acecb0457005)
- [FDA Inspection 893177 - 2014-08-28](https://www.globalkeysolutions.net/records/fda_inspections/phamatech/1fe799a7-159c-4502-af42-52c012917e5a)

Company: https://www.globalkeysolutions.net/companies/phamatech/d9078410-e0ed-43cd-a96c-a20798dd6bfb

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