# FDA Inspection 990162 - LILA CORP - August 12, 2016

Source: https://www.keypedia.com/records/fda_inspections/lila-corp/3c4e8f57-b7e4-4d15-997b-3622c90bd977
Source feed: FDA_Inspections

> FDA Inspection 990162 for LILA CORP on August 12, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 990162
- Company Name: LILA CORP
- Inspection Date: 2016-08-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/lila-corp/416c93bb-8f0e-47d7-8276-9afbe185bb03

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