# FDA Inspection 1000840 - Steripack Asia Sdn Bhd - January 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/steripack-asia-sdn-bhd/9d1c14d2-550f-4cd2-ae38-b674a2d0de91
Source feed: FDA_Inspections

> FDA Inspection 1000840 for Steripack Asia Sdn Bhd on January 24, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000840
- Company Name: Steripack Asia Sdn Bhd
- Inspection Date: 2017-01-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1180197 - 2022-09-01](https://www.keypedia.com/records/fda_inspections/steripack-asia-sdn-bhd/029fc543-e2d6-429e-aadf-a359e89f1654)

Company: https://www.keypedia.com/companies/steripack-asia-sdn-bhd/2dc568db-4d5a-40aa-b262-e938682689eb

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