# FDA Inspection 808901 - Lombart Instrument, Inc. d/b/a Marco Ophthalmic - November 21, 2012

Source: https://www.keypedia.com/records/fda_inspections/lombart-instrument-inc-dba-marco-ophthalmic/ae3e5551-83ee-40da-8cfc-4e594d4c783f
Source feed: FDA_Inspections

> FDA Inspection 808901 for Lombart Instrument, Inc. d/b/a Marco Ophthalmic on November 21, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 808901
- Company Name: Lombart Instrument, Inc. d/b/a Marco Ophthalmic
- Inspection Date: 2012-11-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 808901 - 2012-11-21](https://www.keypedia.com/records/fda_inspections/lombart-instrument-inc-dba-marco-ophthalmic/d7af7c78-3c98-43f1-9507-746cfcce9ced)

Company: https://www.keypedia.com/companies/lombart-instrument-inc-dba-marco-ophthalmic/812aecb9-cb84-4e0c-961c-d1990c1a94f8

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