# FDA Inspection 881039 - Meridian Co., Ltd. - May 29, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/meridian-co-ltd/e53e0063-bfbd-4d61-981b-4fd3dcee0687
Source feed: FDA_Inspections

> FDA Inspection 881039 for Meridian Co., Ltd. on May 29, 2014. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 881039
- Company Name: Meridian Co., Ltd.
- Inspection Date: 2014-05-29
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 881039 - 2014-05-29](https://www.globalkeysolutions.net/records/fda_inspections/meridian-co-ltd/68d3a182-8ea3-4aa6-85d0-6f99054c8b4f)

Company: https://www.globalkeysolutions.net/companies/meridian-co-ltd/cbf6177b-9c18-47ab-9679-cec3d4ef608a

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