prasad1
Active member
Presence of flies in sample storage room, un-calibrated instruments in laboratory and non-adherence to sample analysis procedure were among the lapses found in Ranbaxy's Toansa plant that led to US health regulator FDA banning imports of drugs made at the facility.
According to the report released by the US Food and Drug Administration (FDA) inspection teams, as many as eight lapses were identified, including "too numerous to count (TNTC) flies" in sample storage room, inadequate control over samples and non-adherence of procedures in sample analysis, during their visit to the Toansa, Punjab facility.
Other lapses included usage of un-calibrated and unqualified instruments in laboratory, said the report, which was released two days ago.
According to the report released by the US Food and Drug Administration (FDA) inspection teams, as many as eight lapses were identified, including "too numerous to count (TNTC) flies" in sample storage room, inadequate control over samples and non-adherence of procedures in sample analysis, during their visit to the Toansa, Punjab facility.
Other lapses included usage of un-calibrated and unqualified instruments in laboratory, said the report, which was released two days ago.
