# FDA Inspection 1013486 - ALBERT MEDICAL DEVICES LTD - May 05, 2017

Source: https://www.keypedia.com/records/fda_inspections/albert-medical-devices-ltd/9e37dab1-082a-4af6-8123-0fee64e1a336
Source feed: FDA_Inspections

> FDA Inspection 1013486 for ALBERT MEDICAL DEVICES LTD on May 05, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1013486
- Company Name: ALBERT MEDICAL DEVICES LTD
- Inspection Date: 2017-05-05
- 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 1013486 - 2017-05-05](https://www.keypedia.com/records/fda_inspections/albert-medical-devices-ltd/5c47036b-8378-4c7b-a20a-5f0b32c7f44a)

Company: https://www.keypedia.com/companies/albert-medical-devices-ltd/0b866ed1-a93f-4b3c-8b1a-0082ee50634e

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