# FDA Inspection 730179 - Acare Technology Co., Ltd. - May 04, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/acare-technology-co-ltd/d9677523-cc1e-4560-ae07-dc7c530aa00e
Source feed: FDA_Inspections

> FDA Inspection 730179 for Acare Technology Co., Ltd. on May 04, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 730179
- Company Name: Acare Technology Co., Ltd.
- Inspection Date: 2011-05-04
- 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 846993 - 2013-08-29](https://www.globalkeysolutions.net/records/fda_inspections/acare-technology-co-ltd/1cb3adbf-e096-42ba-bd44-a53d89b9092a)
- [FDA Inspection 730179 - 2011-05-04](https://www.globalkeysolutions.net/records/fda_inspections/acare-technology-co-ltd/5f1a5b63-5985-4ea0-9409-57f191c6e025)

Company: https://www.globalkeysolutions.net/companies/acare-technology-co-ltd/7caf5643-52ce-4d52-8eba-b6afbe096100

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