# Lider – FDA Inspection, May 22, 2025

Source: https://www.keypedia.com/records/fda_inspections/lider/194e8815-9853-45ac-8dd3-d858e626a27b
Source feed: FDA_Inspections

> FDA inspection 1271064 of Lider, May 22, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1271064
- Company Name: Lider
- Inspection Date: 2025-05-22
- 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: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/nikki-s-bryant/fe859d4f-23a6-4bc9-94c6-5b3c3fe8d99a)

Company: https://www.keypedia.com/companies/lider/f9783284-ca7f-499a-9af5-95ea41d1701f

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