# Phamatech – FDA Inspection, Jan 23, 2020

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

> FDA inspection 1117542 of Phamatech, January 23, 2020. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1117542
- Company Name: Phamatech
- Inspection Date: 2020-01-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1262990 - 2025-02-11
- FDA Inspection 1194665 - 2022-12-15
- FDA Inspection 893177 - 2014-08-28

Company: https://www.keypedia.com/companies/phamatech/d9078410-e0ed-43cd-a96c-a20798dd6bfb

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