# FDA Inspection 952122 - BM Korea Co. Ltd. - November 05, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/bm-korea-co-ltd/4bd0d010-d38d-4daf-adae-7dd9465f88d5
Source feed: FDA_Inspections

> FDA Inspection 952122 for BM Korea Co. Ltd. on November 05, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 952122
- Company Name: BM Korea Co. Ltd.
- Inspection Date: 2015-11-05
- 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 1195668 - 2023-01-18](https://www.globalkeysolutions.net/records/fda_inspections/bm-korea-co-ltd/fd69a524-618f-4b03-9a41-e0844e78902e)
- [FDA Inspection 1195668 - 2023-01-18](https://www.globalkeysolutions.net/records/fda_inspections/bm-korea-co-ltd/5fdef33f-f1bd-4778-b2fb-014234bd38d8)
- [FDA Inspection 952122 - 2015-11-05](https://www.globalkeysolutions.net/records/fda_inspections/bm-korea-co-ltd/ef284a20-f3f0-4ab9-bbd1-c182e2731220)

Company: https://www.globalkeysolutions.net/companies/bm-korea-co-ltd/9eaac461-ec3b-444c-9b9c-d7bea5fc2d7b

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