FDA Inspection
Lawton Gmbh & Co. KgLawton Gmbh & Co. Kg – FDA Inspection, May 21, 2016
Record Details
This FDA Inspection record concerns Lawton Gmbh & Co. Kg, with an inspection on May 21, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Lawton Gmbh & Co. Kg
- Inspection Date
- May 21, 2016
- Product Type
- Devices
View Company Profile
ID · ece4d500-1041-4c15-b06b-80295e0b0a7f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 976849
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.198(a)Complaints
- 21 CFR 820.40Lack of procedures, or not maintained
- 21 CFR 820.40(a)Document locations, Dissemination, etc.
- 21 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
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