# FDA Inspection 1229959 - Lenkbar LLC - February 06, 2024

Source: https://www.keypedia.com/records/fda_inspections/lenkbar-llc/6986b991-1c2e-4ed6-99de-b34d225d762e
Source feed: FDA_Inspections

> FDA Inspection 1229959 for Lenkbar LLC on February 06, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1229959
- Company Name: Lenkbar LLC
- Inspection Date: 2024-02-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1229959 - 2024-02-06](https://www.keypedia.com/records/fda_inspections/lenkbar-llc/d823dc5b-5851-4db0-b656-7ba3c6527b56)

Company: https://www.keypedia.com/companies/lenkbar-llc/e040d6a2-2c05-42ec-a0ed-54be8afa42a0

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