# FDA Inspection 890160 - PETER'S TECHNOLOGY (SUZHOU) CO., LTD. - July 24, 2014

Source: https://www.keypedia.com/records/fda_inspections/peters-technology-suzhou-co-ltd/580045fd-61cc-48d6-9b49-ed87e5ef27d7
Source feed: FDA_Inspections

> FDA Inspection 890160 for PETER'S TECHNOLOGY (SUZHOU) CO., LTD. on July 24, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 890160
- Company Name: PETER'S TECHNOLOGY (SUZHOU) CO., LTD.
- Inspection Date: 2014-07-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/peters-technology-suzhou-co-ltd/9e5e4509-5152-4061-8529-d12064fa13e0

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