# FDA Inspection 787759 - Buhl Fijnmetaalbewerking B.V. - June 27, 2012

Source: https://www.keypedia.com/records/fda_inspections/buhl-fijnmetaalbewerking-bv/1de42378-821e-4311-b7aa-4074d0860b74
Source feed: FDA_Inspections

> FDA Inspection 787759 for Buhl Fijnmetaalbewerking B.V. on June 27, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 787759
- Company Name: Buhl Fijnmetaalbewerking B.V.
- Inspection Date: 2012-06-27
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 787759 - 2012-06-27](https://www.keypedia.com/records/fda_inspections/buhl-fijnmetaalbewerking-bv/5b440728-7636-4aa1-a857-99be88cd7439)
- [FDA Inspection 787759 - 2012-06-27](https://www.keypedia.com/records/fda_inspections/buhl-fijnmetaalbewerking-bv/312740af-d6a9-4693-9a94-4726f2c891da)
- [FDA Inspection 575441 - 2009-04-02](https://www.keypedia.com/records/fda_inspections/buhl-fijnmetaalbewerking-bv/5ec97b87-d3ea-4de8-8022-65d3381da32d)

Company: https://www.keypedia.com/companies/buhl-fijnmetaalbewerking-bv/7ba40ab1-d9b9-4d7e-ad7f-e52319d72a82

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