# OPTILASA, S.L. – FDA Inspection, Oct 27, 2022

Source: https://www.keypedia.com/records/fda_inspections/optilasa-sl/dd7b124b-e318-44b4-9cca-736a2c79f1c6
Source feed: FDA_Inspections

> FDA inspection 1182109 of OPTILASA, S.L., October 27, 2022. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1182109
- Company Name: OPTILASA, S.L.
- Inspection Date: 2022-10-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 1045855 - 2018-02-01
- FDA Inspection 839603 - 2013-07-11
- [FDA Inspection 669185 - 2010-06-02](https://www.keypedia.com/records/fda_inspections/optilasa-sl/aea415f2-fd03-4be6-90a6-84ad1099b201)

Company: https://www.keypedia.com/companies/optilasa-sl/ba70429d-334c-4ee4-9c1d-6fae685424e3

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