# FDA Inspection 864181 - PROMEPLA - December 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/promepla/39e2bbaf-783e-4d37-acdc-de7bed8142f4
Source feed: FDA_Inspections

> FDA Inspection 864181 for PROMEPLA on December 12, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 864181
- Company Name: PROMEPLA
- Inspection Date: 2013-12-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/promepla/e75790ce-8af4-4a01-8612-f6d7f462cfc3

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