# OPTILASA, S.L. – FDA Inspection, Jun 2, 2010

Source: https://www.keypedia.com/records/fda_inspections/optilasa-sl/aea415f2-fd03-4be6-90a6-84ad1099b201
Source feed: FDA_Inspections

> FDA inspection 669185 of OPTILASA, S.L., June 02, 2010. Classification: Official Action Indicated (OAI). 13 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 669185
- Company Name: OPTILASA, S.L.
- Inspection Date: 2010-06-02
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 13

## Related Documents

- [FDA Inspection 1182109 - 2022-10-27](https://www.keypedia.com/records/fda_inspections/optilasa-sl/dd7b124b-e318-44b4-9cca-736a2c79f1c6)
- FDA Inspection 1045855 - 2018-02-01
- FDA Inspection 839603 - 2013-07-11

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