FDA Inspection 935786 — Sagami Manufacturers Sdn. Bhd.

Sagami Manufacturers Sdn. Bhd. — FEI 3005664717

The FDA completed an inspection of Sagami Manufacturers Sdn. Bhd. on July 2, 2015 in Batu Gajah. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 2, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Batu Gajah (Malaysia)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures