# FDA Inspection 878762 - L & R Mfg Co - May 13, 2014

Source: https://www.keypedia.com/records/fda_inspections/l-r-mfg-co/8933386e-5881-49c4-b1ef-ba20c5c10d2e
Source feed: FDA_Inspections

> FDA Inspection 878762 for L & R Mfg Co on May 13, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 878762
- Company Name: L & R Mfg Co
- Inspection Date: 2014-05-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 878762 - 2014-05-13](https://www.keypedia.com/records/fda_inspections/l-r-mfg-co/7f6c8240-9113-4f7e-997f-7b2a52b1371b)

Company: https://www.keypedia.com/companies/l-r-mfg-co/033ab05c-0508-4c89-858f-24f2c17d4721

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