# FDA Inspection 987184 - BRIGHTWAKE LTD - August 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/brightwake-ltd/f561a9cc-2623-4770-aad6-a191b8202db9
Source feed: FDA_Inspections

> FDA Inspection 987184 for BRIGHTWAKE LTD on August 19, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987184
- Company Name: BRIGHTWAKE LTD
- Inspection Date: 2016-08-19
- 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/brightwake-ltd/3aff99da-0177-40f6-ab12-88a1fbd818a2

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