# FDA Inspection 848920 - Moog Costa Rica, SRL - September 19, 2013

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

> FDA Inspection 848920 for Moog Costa Rica, SRL on September 19, 2013. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 848920
- Company Name: Moog Costa Rica, SRL
- Inspection Date: 2013-09-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1070560 - 2018-11-01](https://www.globalkeysolutions.net/api/records/fda_inspections/moog-costa-rica-srl/3ab4aecf-cdb4-4e57-b857-d91bfef24da7/)
- [FDA Inspection 970327 - 2016-04-28](https://www.globalkeysolutions.net/api/records/fda_inspections/moog-costa-rica-srl/fb140976-c8e6-4da9-b043-34918b6ce541/)
- [FDA Inspection 970327 - 2016-04-28](https://www.globalkeysolutions.net/api/records/fda_inspections/moog-costa-rica-srl/acf07aab-7279-4c87-a576-cf08afe26cd7/)

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

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