# GMDASZ Manufacturing Co., Ltd. – FDA Inspection, Jan 29, 2015

Source: https://www.keypedia.com/records/fda_inspections/gmdasz-manufacturing-co-ltd/de580d54-08f1-4531-b094-babfa6928a92
Source feed: FDA_Inspections

> FDA inspection 913245 of GMDASZ Manufacturing Co., Ltd., January 29, 2015. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 913245
- Company Name: GMDASZ Manufacturing Co., Ltd.
- Inspection Date: 2015-01-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1121461 - 2019-08-15](https://www.keypedia.com/records/fda_inspections/gmdasz-manufacturing-co-ltd/44a45d53-23ce-48d9-8ffb-73e54558386b)
- [FDA Inspection 1039827 - 2018-01-18](https://www.keypedia.com/records/fda_inspections/gmdasz-manufacturing-co-ltd/69e6328b-7922-463d-9d19-7cdb0967f929)

Company: https://www.keypedia.com/companies/gmdasz-manufacturing-co-ltd/75d937ba-3c69-457e-bbe6-d1c04ee4c9ae

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