# FDA Inspection 1099650 - Greatbatch Medical  S. De R.L. De C.V. - August 15, 2019

Source: https://www.keypedia.com/records/fda_inspections/greatbatch-medical-s-de-rl-de-cv/2c89199e-66c4-47bf-a793-5706f4dee807
Source feed: FDA_Inspections

> FDA Inspection 1099650 for Greatbatch Medical  S. De R.L. De C.V. on August 15, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099650
- Company Name: Greatbatch Medical  S. De R.L. De C.V.
- Inspection Date: 2019-08-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1199725 - 2023-02-02](https://www.keypedia.com/records/fda_inspections/greatbatch-medical-s-de-rl-de-cv/ea2e8ced-99cf-4d43-babf-020d5568e189)

Company: https://www.keypedia.com/companies/greatbatch-medical-s-de-rl-de-cv/d99c9bd8-e056-4cb2-85b8-5c6d7df1c41c

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