# Moog Costa Rica, SRL – FDA Inspection, Sep 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/moog-costa-rica-srl/fca86433-63ea-41a1-a6f4-8e8a86a9ea63
Source feed: FDA_Inspections

> FDA inspection 848920 of Moog Costa Rica, SRL, September 19, 2013. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 848920
- Company Name: Moog Costa Rica, SRL
- Inspection Date: 2013-09-19
- 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: 1

## Related Documents

- [FDA Inspection 1070560 - 2018-11-01](https://www.keypedia.com/records/fda_inspections/moog-costa-rica-srl/3ab4aecf-cdb4-4e57-b857-d91bfef24da7)
- [FDA Inspection 970327 - 2016-04-28](https://www.keypedia.com/records/fda_inspections/moog-costa-rica-srl/fb140976-c8e6-4da9-b043-34918b6ce541)

Company: https://www.keypedia.com/companies/moog-costa-rica-srl/051536ac-f843-426f-b5a6-4805d1e99826

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