# FDA Inspection 1311480 - Medcraft LLC - April 08, 2026

Source: https://www.globalkeysolutions.net/records/fda_inspections/medcraft-llc/d4a15939-7d9d-41a0-8001-897a55bb4104
Source feed: FDA_Inspections

> FDA Inspection 1311480 for Medcraft LLC on April 08, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1311480
- Company Name: Medcraft LLC
- Inspection Date: 2026-04-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1311480 - 2026-04-08](https://www.globalkeysolutions.net/records/fda_inspections/medcraft-llc/9e36faa8-28d0-4930-b064-37ff16107260)
- [FDA Inspection 1060228 - 2018-07-27](https://www.globalkeysolutions.net/records/fda_inspections/medcraft-llc/8467305d-7121-441d-94b5-b205cfa58b2c)

Company: https://www.globalkeysolutions.net/companies/medcraft-llc/e9a4ae52-ddc4-4dd5-8dec-12e41a756277

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