# NARVA Lichtquelle GmbH + Co. KG – FDA Inspection, Jul 29, 2016

Source: https://www.keypedia.com/records/fda_inspections/narva-lichtquelle-gmbh-co-kg/7539e8b4-c208-453a-b022-d9350de79416
Source feed: FDA_Inspections

> FDA inspection 981931 of NARVA Lichtquelle GmbH + Co. KG, July 29, 2016. Classification: Official Action Indicated (OAI). 10 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 981931
- Company Name: NARVA Lichtquelle GmbH + Co. KG
- Inspection Date: 2016-07-29
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

## Related Documents

- [FDA Inspection 1199457 - 2023-02-22](https://www.keypedia.com/records/fda_inspections/narva-lichtquelle-gmbh-co-kg/5723a647-7de1-4d41-8e4d-29f39ba5eb46)
- [FDA Inspection 1027652 - 2017-09-28](https://www.keypedia.com/records/fda_inspections/narva-lichtquelle-gmbh-co-kg/54d31587-cfe9-48f5-9713-f03fb72536b4)

Company: https://www.keypedia.com/companies/narva-lichtquelle-gmbh-co-kg/6b216816-4dd4-448a-9dba-62e181ffd2ca

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