# EPS Bio Technology Corp. – FDA Inspection, Oct 26, 2023

Source: https://www.keypedia.com/records/fda_inspections/eps-bio-technology-corp/596efedf-201d-4497-9163-efe64bb73548
Source feed: FDA_Inspections

> FDA inspection 1227391 of EPS Bio Technology Corp., October 26, 2023. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1227391
- Company Name: EPS Bio Technology Corp.
- Inspection Date: 2023-10-26
- 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: 0

## Related Documents

- [FDA Inspection 1299020 - 2026-01-15](https://www.keypedia.com/records/fda_inspections/eps-bio-technology-corp/bd75facd-afdb-491e-a6a0-7265abac84a8)
- FDA Inspection 1116987 - 2020-01-08
- FDA Inspection 845943 - 2013-07-26
- [FDA Inspection 789179 - 2012-06-21](https://www.keypedia.com/records/fda_inspections/eps-bio-technology-corp/aef9083c-343c-47ca-89e3-69d7280ba370)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/felix-j-marrero/fe3bf64e-987b-40d9-8a17-754d58e13433)

Company: https://www.keypedia.com/companies/eps-bio-technology-corp/bb3026bd-46a6-4a6f-b8e0-2bbc1adfe0fb

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