# Implanet S.A. – FDA Inspection, Jul 4, 2025

Source: https://www.keypedia.com/records/fda_inspections/implanet-sa/9a128340-1f2d-43b3-bdf6-6ec7938fbe02
Source feed: FDA_Inspections

> FDA inspection 1276580 of Implanet S.A., July 04, 2025. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276580
- Company Name: Implanet S.A.
- Inspection Date: 2025-07-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Documents

- FDA Inspection 996165 - 2016-10-19
- FDA Inspection 866660 - 2014-02-06

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/albert-l-nguyen/496338d0-71c4-43da-92f0-09515559d9fc)

Company: https://www.keypedia.com/companies/implanet-sa/0f19064d-5601-4caf-a4d6-9a140afdd8d0

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8